Canonical Allele Identifier: CA1865483081

Gene: FANCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.95171057G= , CM000671.2:g.95171057G=	GRCh38
NC_000009.11:g.97933339G= , CM000671.1:g.97933339G=	GRCh37
NC_000009.10:g.96973160G=	NCBI36
NG_011707.1:g.151653C= , LRG_497:g.151653C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000696261.1:n.912+22C=
ENST00000289081.8:c.521+22C= MANE Select	ENSP00000289081.3:n.521+22C=
ENST00000375305.6:c.521+22C=	ENSP00000364454.1:n.521+22C=
ENST00000490972.7:c.521+22C=	ENSP00000479931.1:n.521+22C=
ENST00000636777.1:n.579+22C=
ENST00000649334.1:c.666+22C=	ENSP00000497735.1:n.666+22C=
ENST00000649701.1:n.236+22C=
ENST00000289081.7:c.521+22C=	ENSP00000289081.3:n.521+22C=
ENST00000375305.5:c.521+22C=	ENSP00000364454.1:n.521+22C=
ENST00000490972.6:c.521+22C=	ENSP00000479931.1:n.521+22C=
NM_000136.2:c.521+22C= , LRG_497t1:c.521+22C=	NP_000127.2:n.521+22C=
NM_001243743.1:c.521+22C=	NP_001230672.1:n.521+22C=
NM_001243744.1:c.521+22C=	NP_001230673.1:n.521+22C=
XM_006717001.1:c.521+22C=	XP_006717064.1:n.521+22C=
XM_006717002.2:c.521+22C=	XP_006717065.1:n.521+22C=
XM_006717004.2:c.521+22C=	XP_006717067.1:n.521+22C=
XM_011518365.1:c.521+22C=	XP_011516667.1:n.521+22C=
XM_011518366.1:c.521+22C=	XP_011516668.1:n.521+22C=
XM_011518367.1:c.65+22C=	XP_011516669.1:n.65+22C=
XM_006717001.3:c.521+22C=	XP_006717064.1:n.521+22C=
XM_006717002.4:c.521+22C=	XP_006717065.1:n.521+22C=
XM_006717004.4:c.521+22C=	XP_006717067.1:n.521+22C=
XM_011518365.3:c.521+22C=	XP_011516667.1:n.521+22C=
XM_011518366.3:c.521+22C=	XP_011516668.1:n.521+22C=
XM_011518367.2:c.65+22C=	XP_011516669.1:n.65+22C=
XM_017014452.2:c.65+22C=	XP_016869941.1:n.65+22C=
XM_017014453.1:c.65+22C=	XP_016869942.1:n.65+22C=
XM_017014454.1:c.65+22C=	XP_016869943.1:n.65+22C=
XM_024447451.1:c.521+22C=	XP_024303219.1:n.521+22C=
NM_000136.3:c.521+22C= MANE Select	NP_000127.2:n.521+22C=
NM_001243743.2:c.521+22C=	NP_001230672.1:n.521+22C=
NM_001243744.2:c.521+22C=	NP_001230673.1:n.521+22C=