Canonical Allele Identifier: CA1474916716
Gene: FAM13A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.88820118G= , CM000666.2:g.88820118G= GRCh38
NC_000004.11:g.89741269G= , CM000666.1:g.89741269G= GRCh37
NC_000004.10:g.89960292G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014883.4:c.1008-15066C= MANE Select NP_055698.2:n.1008-15066C=
ENST00000264344.10:c.1008-15066C= MANE Select ENSP00000264344.5:n.1008-15066C=
NM_001015045.2:c.29+2858C= NP_001015045.1:n.29+2858C=
NM_001015045.3:c.29+2858C= NP_001015045.1:n.29+2858C=
NM_001265578.1:c.29+2858C= NP_001252507.1:n.29+2858C=
NM_001265578.2:c.29+2858C= NP_001252507.1:n.29+2858C=
NM_001265579.1:c.29+2858C= NP_001252508.1:n.29+2858C=
NM_001265579.2:c.29+2858C= NP_001252508.1:n.29+2858C=
NM_001265580.1:c.29+2858C= NP_001252509.1:n.29+2858C=
NM_001265580.2:c.29+2858C= NP_001252509.1:n.29+2858C=
NM_014883.3:c.1008-15066C= NP_055698.2:n.1008-15066C=
ENST00000264344.9:c.1008-15066C= ENSP00000264344.5:n.1008-15066C=
ENST00000395002.6:c.29+2858C= ENSP00000378450.2:n.29+2858C=
ENST00000502459.5:n.1466-15066C=
ENST00000503556.5:c.29+2858C= ENSP00000427189.1:n.29+2858C=
ENST00000504836.5:c.29+2858C= ENSP00000427077.1:n.29+2858C=
ENST00000507352.1:c.29+2858C= ENSP00000425784.1:n.29+2858C=
ENST00000508369.5:c.29+2858C= ENSP00000421562.1:n.29+2858C=
ENST00000511976.5:c.217-52059C= ENSP00000421914.1:n.217-52059C=
ENST00000513837.5:c.29+2858C= ENSP00000423252.1:n.29+2858C=
XM_005262681.2:c.1008-29491C= XP_005262738.1:n.1008-29491C=
XM_005262681.3:c.1008-29491C= XP_005262738.1:n.1008-29491C=
XM_005262682.2:c.948-15066C= XP_005262739.1:n.948-15066C=
XM_005262683.2:c.1008-15066C= XP_005262740.1:n.1008-15066C=
XM_005262683.3:c.1008-15066C= XP_005262740.1:n.1008-15066C=
XM_005262684.2:c.381-15066C= XP_005262741.1:n.381-15066C=
XM_005262684.4:c.381-15066C= XP_005262741.1:n.381-15066C=
XM_006714057.2:c.441-15066C= XP_006714120.1:n.441-15066C=
XM_006714057.3:c.441-15066C= XP_006714120.1:n.441-15066C=
XM_011531516.1:c.1008-15066C= XP_011529818.1:n.1008-15066C=
XM_011531517.1:c.924-15066C= XP_011529819.1:n.924-15066C=
XM_011531517.2:c.924-15066C= XP_011529819.1:n.924-15066C=
XM_011531518.1:c.450-15066C= XP_011529820.1:n.450-15066C=
XM_011531519.1:c.450-15066C= XP_011529821.1:n.450-15066C=
XM_011531519.3:c.450-15066C= XP_011529821.1:n.450-15066C=
XM_011531520.1:c.381-15066C= XP_011529822.1:n.381-15066C=
XM_017007624.2:c.1008-29491C= XP_016863113.1:n.1008-29491C=
XM_017007625.1:c.843-15066C= XP_016863114.1:n.843-15066C=
XM_017007626.1:c.477-15066C= XP_016863115.1:n.477-15066C=
XM_017007627.1:c.381-15066C= XP_016863116.1:n.381-15066C=
XM_017007628.2:c.381-29491C= XP_016863117.1:n.381-29491C=
XM_017007629.2:c.192-15066C= XP_016863118.1:n.192-15066C=
XM_017007630.2:c.192-15066C= XP_016863119.1:n.192-15066C=
XM_017007631.2:c.192-29491C= XP_016863120.1:n.192-29491C=
XM_017007632.2:c.192-29491C= XP_016863121.1:n.192-29491C=
XM_017007633.2:c.45-15066C= XP_016863122.1:n.45-15066C=
XM_017007634.2:c.29+2858C= XP_016863123.1:n.29+2858C=
XM_024453870.1:c.1008-15066C= XP_024309638.1:n.1008-15066C=