Canonical Allele Identifier: CA1474948510
Gene: FAM13A HGNC NCBI

Linked Data

dbSNP Id: rs1745091701

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88890100_88890101insTAAAAACAAAACTGAACTACATT , CM000666.2:g.88890100_88890101insTAAAAACAAAACTGAACTACATT GRCh38
NC_000004.11:g.89811251_89811252insTAAAAACAAAACTGAACTACATT , CM000666.1:g.89811251_89811252insTAAAAACAAAACTGAACTACATT GRCh37
NC_000004.10:g.90030274_90030275insTAAAAACAAAACTGAACTACATT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000264344.10:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA MANE Select ENSP00000264344.5:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTT...
ENST00000264344.9:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA ENSP00000264344.5:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTT...
ENST00000502459.5:n.1301+16278_1301+16279insAATGTAGTTCAGTTTTGTTTTTA
ENST00000511145.1:n.226+15585_226+15586insAATGTAGTTCAGTTTTGTTTTTA
ENST00000511976.5:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA ENSP00000421914.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTT...
ENST00000512339.5:c.*212+16278_*212+16279insAATGTAGTTCAGTTTTGTTTTTA ENSP00000423800.1:n.*212+16278_*212+16279insAATGTAGTTCAGTTTTG...
NM_014883.3:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA NP_055698.2:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA
XM_005262681.2:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262738.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262682.2:c.783+16278_783+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262739.1:n.783+16278_783+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262683.2:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262740.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262684.2:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262741.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_006714057.2:c.276+16278_276+16279insAATGTAGTTCAGTTTTGTTTTTA XP_006714120.1:n.276+16278_276+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_011531516.1:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_011529818.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_011531517.1:c.760-38918_760-38917insAATGTAGTTCAGTTTTGTTTTTA XP_011529819.1:n.760-38918_760-38917insAATGTAGTTCAGTTTTGTTTTT...
XM_011531518.1:c.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTTA XP_011529820.1:n.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_011531519.1:c.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTTA XP_011529821.1:n.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_011531520.1:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA XP_011529822.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262681.3:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262738.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262683.3:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262740.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_005262684.4:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA XP_005262741.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_006714057.3:c.276+16278_276+16279insAATGTAGTTCAGTTTTGTTTTTA XP_006714120.1:n.276+16278_276+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_011531517.2:c.760-38918_760-38917insAATGTAGTTCAGTTTTGTTTTTA XP_011529819.1:n.760-38918_760-38917insAATGTAGTTCAGTTTTGTTTTT...
XM_011531519.3:c.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTTA XP_011529821.1:n.285+16278_285+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007624.2:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863113.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007625.1:c.678+16278_678+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863114.1:n.678+16278_678+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007626.1:c.312+16278_312+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863115.1:n.312+16278_312+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007627.1:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863116.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007628.2:c.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863117.1:n.216+16278_216+16279insAATGTAGTTCAGTTTTGTTTTT...
XM_017007629.2:c.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863118.1:n.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA
XM_017007630.2:c.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863119.1:n.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA
XM_017007631.2:c.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863120.1:n.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA
XM_017007632.2:c.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA XP_016863121.1:n.27+16278_27+16279insAATGTAGTTCAGTTTTGTTTTTA
XM_017007633.2:c.-120-38918_-120-38917insAATGTAGTTCAGTTTTGTTTTTA XP_016863122.1:n.-120-38918_-120-38917insAATGTAGTTCAGTTTTGTTT...
XM_024453870.1:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA XP_024309638.1:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTT...
NM_014883.4:c.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA MANE Select NP_055698.2:n.843+16278_843+16279insAATGTAGTTCAGTTTTGTTTTTA