Canonical Allele Identifier: CA15631463

Gene: FAM13C

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59360724C>T , CM000672.2:g.59360724C>T	GRCh38
NC_000010.10:g.61120484C>T , CM000672.1:g.61120484C>T	GRCh37
NC_000010.9:g.60790490C>T	NCBI36
NG_053188.1:g.7463G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000618804.5:c.62+1675G>A MANE Select	ENSP00000481854.1:n.62+1675G>A
ENST00000422313.6:c.62+1675G>A	ENSP00000400241.2:n.62+1675G>A
ENST00000435852.6:c.62+1675G>A	ENSP00000392302.2:n.62+1675G>A
ENST00000468840.6:c.-188+1675G>A	ENSP00000423896.1:n.-188+1675G>A
ENST00000470220.5:n.165+1675G>A
ENST00000503444.1:c.-188+302G>A	ENSP00000424797.1:n.-188+302G>A
ENST00000512919.5:c.-188+302G>A	ENSP00000425820.1:n.-188+302G>A
ENST00000611933.4:c.62+1675G>A	ENSP00000481830.1:n.62+1675G>A
ENST00000614220.4:c.62+1675G>A	ENSP00000483510.1:n.62+1675G>A
ENST00000618427.4:c.-188+302G>A	ENSP00000480677.1:n.-188+302G>A
ENST00000618804.4:c.62+1675G>A	ENSP00000481854.1:n.62+1675G>A
ENST00000619059.4:c.147+302G>A	ENSP00000484965.1:n.147+302G>A
ENST00000621119.4:c.62+1675G>A	ENSP00000484625.1:n.62+1675G>A
ENST00000622363.4:c.147+302G>A	ENSP00000484539.1:n.147+302G>A
NM_001001971.2:c.62+1675G>A	NP_001001971.1:n.62+1675G>A
NM_001143773.1:c.-188+1675G>A	NP_001137245.1:n.-188+1675G>A
NM_001166698.1:c.-188+302G>A	NP_001160170.1:n.-188+302G>A
NM_198215.3:c.62+1675G>A	NP_937858.2:n.62+1675G>A
XM_005269618.3:c.62+1675G>A	XP_005269675.2:n.62+1675G>A
XM_005269619.3:c.62+1675G>A	XP_005269676.2:n.62+1675G>A
XM_006717702.2:c.-188+302G>A	XP_006717765.1:n.-188+302G>A
XM_006717703.2:c.-188+302G>A	XP_006717766.1:n.-188+302G>A
XM_011539489.1:c.-188+302G>A	XP_011537791.1:n.-188+302G>A
XM_011539490.1:c.-304+1675G>A	XP_011537792.1:n.-304+1675G>A
XM_011539491.1:c.-304+302G>A	XP_011537793.1:n.-304+302G>A
NM_001347840.1:c.-188+1675G>A	NP_001334769.1:n.-188+1675G>A
NM_001347842.1:c.-188+1675G>A	NP_001334771.1:n.-188+1675G>A
NM_001347843.1:c.-304+302G>A	NP_001334772.1:n.-304+302G>A
NM_001347844.1:c.-188+302G>A	NP_001334773.1:n.-188+302G>A
NM_001347845.1:c.-188+1675G>A	NP_001334774.1:n.-188+1675G>A
NM_001347846.1:c.-188+1675G>A	NP_001334775.1:n.-188+1675G>A
NM_001347847.1:c.-188+302G>A	NP_001334776.1:n.-188+302G>A
NM_001347848.1:c.-304+1675G>A	NP_001334777.1:n.-304+1675G>A
NM_001347849.1:c.62+1675G>A	NP_001334778.1:n.62+1675G>A
NM_001347850.1:c.-304+1675G>A	NP_001334779.1:n.-304+1675G>A
NM_001347851.1:c.-188+302G>A	NP_001334780.1:n.-188+302G>A
NM_001347852.1:c.62+1675G>A	NP_001334781.1:n.62+1675G>A
XM_005269618.4:c.62+1675G>A	XP_005269675.2:n.62+1675G>A
XM_005269619.4:c.62+1675G>A	XP_005269676.2:n.62+1675G>A
XM_006717702.3:c.-188+302G>A	XP_006717765.1:n.-188+302G>A
XM_011539490.2:c.-304+1675G>A	XP_011537792.1:n.-304+1675G>A
XM_011539491.2:c.-304+302G>A	XP_011537793.1:n.-304+302G>A
XM_017015886.1:c.-188+1675G>A	XP_016871375.1:n.-188+1675G>A
XM_017015889.1:c.-188+302G>A	XP_016871378.1:n.-188+302G>A
XM_017015891.1:c.-188+1675G>A	XP_016871380.1:n.-188+1675G>A
XM_024447879.1:c.-304+1675G>A	XP_024303647.1:n.-304+1675G>A
NM_198215.4:c.62+1675G>A MANE Select	NP_937858.2:n.62+1675G>A
NM_001001971.3:c.62+1675G>A	NP_001001971.1:n.62+1675G>A
NM_001166698.2:c.-188+302G>A	NP_001160170.1:n.-188+302G>A
NM_001347840.2:c.-188+1675G>A	NP_001334769.1:n.-188+1675G>A
NM_001347842.2:c.-188+1675G>A	NP_001334771.1:n.-188+1675G>A
NM_001347849.2:c.62+1675G>A	NP_001334778.1:n.62+1675G>A
NM_001347850.2:c.-304+1675G>A	NP_001334779.1:n.-304+1675G>A
NM_001347851.2:c.-188+302G>A	NP_001334780.1:n.-188+302G>A
NM_001347852.2:c.62+1675G>A	NP_001334781.1:n.62+1675G>A