Canonical Allele Identifier: CA449942252

Gene: FANCE

Linked Data

• gnomAD v4: 6-35455756-G-A
• MyVariant Identifiers: chr6:g.35423533G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455756G>A , CM000668.2:g.35455756G>A	GRCh38
NC_000006.11:g.35423533G>A , CM000668.1:g.35423533G>A	GRCh37
NC_000006.10:g.35531511G>A	NCBI36
NG_011708.1:g.8396G>A , LRG_498:g.8396G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.258G>A	ENSP00000512511.1:p.Leu86=
ENST00000696265.1:c.258G>A	ENSP00000512512.1:p.Leu86=
ENST00000229769.3:c.258G>A MANE Select	ENSP00000229769.2:p.Leu86=
ENST00000648059.1:c.258G>A	ENSP00000497902.1:p.Leu86=
ENST00000229769.2:c.258G>A	ENSP00000229769.2:p.Leu86=
NM_021922.2:c.258G>A , LRG_498t1:c.258G>A	NP_068741.1:p.Leu86=
XM_005248885.2:c.258G>A	XP_005248942.1:p.Leu86=
XM_005248886.2:c.258G>A	XP_005248943.1:p.Leu86=
XM_005248887.2:c.258G>A	XP_005248944.1:p.Leu86=
XM_005248888.2:c.258G>A	XP_005248945.1:p.Leu86=
XM_011514343.1:c.-37G>A	XP_011512645.1:n.-37G>A
XM_011514344.1:c.-37G>A	XP_011512646.1:n.-37G>A
XM_005248888.3:c.258G>A	XP_005248945.1:p.Leu86=
XM_011514343.2:c.-37G>A	XP_011512645.1:n.-37G>A
XR_001743226.1:n.465G>A
XR_002956267.1:n.465G>A
NM_021922.3:c.258G>A MANE Select	NP_068741.1:p.Leu86=