Canonical Allele Identifier: CA100973035

Gene: FAM13A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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