Canonical Allele Identifier: CA1620905543

Gene: FANCE

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456049C= , CM000668.2:g.35456049C=	GRCh38
NC_000006.11:g.35423826C= , CM000668.1:g.35423826C=	GRCh37
NC_000006.10:g.35531804C=	NCBI36
NG_011708.1:g.8689C= , LRG_498:g.8689C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.551C=	ENSP00000512511.1:p.Pro184=
ENST00000696265.1:c.551C=	ENSP00000512512.1:p.Pro184=
ENST00000696266.1:c.269C=	ENSP00000512513.1:p.Pro90=
ENST00000696267.1:n.191C=
ENST00000229769.3:c.551C= MANE Select	ENSP00000229769.2:p.Pro184=
ENST00000648059.1:c.551C=	ENSP00000497902.1:p.Pro184=
ENST00000229769.2:c.551C=	ENSP00000229769.2:p.Pro184=
NM_021922.2:c.551C= , LRG_498t1:c.551C=	NP_068741.1:p.Pro184=
XM_005248885.2:c.551C=	XP_005248942.1:p.Pro184=
XM_005248886.2:c.551C=	XP_005248943.1:p.Pro184=
XM_005248887.2:c.551C=	XP_005248944.1:p.Pro184=
XM_005248888.2:c.551C=	XP_005248945.1:p.Pro184=
XM_011514343.1:c.257C=	XP_011512645.1:p.Pro86=
XM_011514344.1:c.257C=	XP_011512646.1:p.Pro86=
XM_005248888.3:c.551C=	XP_005248945.1:p.Pro184=
XM_011514343.2:c.257C=	XP_011512645.1:p.Pro86=
XR_001743226.1:n.758C=
XR_002956267.1:n.758C=
NM_021922.3:c.551C= MANE Select	NP_068741.1:p.Pro184=