Canonical Allele Identifier: CA450123843

Gene: FANCE

Linked Data

• gnomAD v4: 6-35456137-G-T
• MyVariant Identifiers: chr6:g.35423914G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35456137G>T , CM000668.2:g.35456137G>T	GRCh38
NC_000006.11:g.35423914G>T , CM000668.1:g.35423914G>T	GRCh37
NC_000006.10:g.35531892G>T	NCBI36
NG_011708.1:g.8777G>T , LRG_498:g.8777G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.639G>T	ENSP00000512511.1:p.Gly213=
ENST00000696265.1:c.639G>T	ENSP00000512512.1:p.Gly213=
ENST00000696266.1:c.357G>T	ENSP00000512513.1:p.Gly119=
ENST00000696267.1:n.279G>T
ENST00000229769.3:c.639G>T MANE Select	ENSP00000229769.2:p.Gly213=
ENST00000648059.1:c.639G>T	ENSP00000497902.1:p.Gly213=
ENST00000229769.2:c.639G>T	ENSP00000229769.2:p.Gly213=
NM_021922.2:c.639G>T , LRG_498t1:c.639G>T	NP_068741.1:p.Gly213=
XM_005248885.2:c.639G>T	XP_005248942.1:p.Gly213=
XM_005248886.2:c.639G>T	XP_005248943.1:p.Gly213=
XM_005248887.2:c.639G>T	XP_005248944.1:p.Gly213=
XM_005248888.2:c.639G>T	XP_005248945.1:p.Gly213=
XM_011514343.1:c.345G>T	XP_011512645.1:p.Gly115=
XM_011514344.1:c.345G>T	XP_011512646.1:p.Gly115=
XM_005248888.3:c.639G>T	XP_005248945.1:p.Gly213=
XM_011514343.2:c.345G>T	XP_011512645.1:p.Gly115=
XR_001743226.1:n.846G>T
XR_002956267.1:n.846G>T
NM_021922.3:c.639G>T MANE Select	NP_068741.1:p.Gly213=