Canonical Allele Identifier: CA1865483587

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95172077C= , CM000671.2:g.95172077C=	GRCh38
NC_000009.11:g.97934359C= , CM000671.1:g.97934359C=	GRCh37
NC_000009.10:g.96974180C=	NCBI36
NG_011707.1:g.150633G= , LRG_497:g.150633G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696261.1:n.807G=
ENST00000289081.8:c.416G= MANE Select	ENSP00000289081.3:p.Gly139=
ENST00000375305.6:c.416G=	ENSP00000364454.1:p.Gly139=
ENST00000490972.7:c.416G=	ENSP00000479931.1:p.Gly139=
ENST00000636777.1:n.474G=
ENST00000647778.1:c.416G=	ENSP00000498125.1:p.Gly139=
ENST00000649334.1:c.561G=	ENSP00000497735.1:n.561G=
ENST00000649701.1:n.131G=
ENST00000289081.7:c.416G=	ENSP00000289081.3:p.Gly139=
ENST00000375305.5:c.416G=	ENSP00000364454.1:p.Gly139=
ENST00000433829.1:c.416G=	ENSP00000406908.1:p.Gly139=
ENST00000474949.1:n.773G=
ENST00000490972.6:c.416G=	ENSP00000479931.1:p.Gly139=
NM_000136.2:c.416G= , LRG_497t1:c.416G=	NP_000127.2:p.Gly139=
NM_001243743.1:c.416G=	NP_001230672.1:p.Gly139=
NM_001243744.1:c.416G=	NP_001230673.1:p.Gly139=
XM_006717001.1:c.416G=	XP_006717064.1:p.Gly139=
XM_006717002.2:c.416G=	XP_006717065.1:p.Gly139=
XM_006717004.2:c.416G=	XP_006717067.1:p.Gly139=
XM_011518365.1:c.416G=	XP_011516667.1:p.Gly139=
XM_011518366.1:c.416G=	XP_011516668.1:p.Gly139=
XM_011518367.1:c.-41G=	XP_011516669.1:n.-41G=
XM_006717001.3:c.416G=	XP_006717064.1:p.Gly139=
XM_006717002.4:c.416G=	XP_006717065.1:p.Gly139=
XM_006717004.4:c.416G=	XP_006717067.1:p.Gly139=
XM_011518365.3:c.416G=	XP_011516667.1:p.Gly139=
XM_011518366.3:c.416G=	XP_011516668.1:p.Gly139=
XM_011518367.2:c.-41G=	XP_011516669.1:n.-41G=
XM_017014452.2:c.-41G=	XP_016869941.1:n.-41G=
XM_017014453.1:c.-41G=	XP_016869942.1:n.-41G=
XM_017014454.1:c.-41G=	XP_016869943.1:n.-41G=
XM_024447451.1:c.416G=	XP_024303219.1:p.Gly139=
NM_000136.3:c.416G= MANE Select	NP_000127.2:p.Gly139=
NM_001243743.2:c.416G=	NP_001230672.1:p.Gly139=
NM_001243744.2:c.416G=	NP_001230673.1:p.Gly139=