Canonical Allele Identifier: CA3771390

Gene: FANCE

Linked Data

• ClinVar Variation Id: 1034828
• ClinVar RCV Id: RCV001337606
• dbSNP Id: rs757051494
• ExAC: 6:35423605 G / A
• gnomAD v2: 6-35423605-G-A
• gnomAD v3: 6-35455828-G-A
• gnomAD v4: 6-35455828-G-A
• MyVariant Identifiers: chr6:g.35423605G>A (hg19) ; chr6:g.35455828G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455828G>A , CM000668.2:g.35455828G>A	GRCh38
NC_000006.11:g.35423605G>A , CM000668.1:g.35423605G>A	GRCh37
NC_000006.10:g.35531583G>A	NCBI36
NG_011708.1:g.8468G>A , LRG_498:g.8468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.330G>A	ENSP00000512511.1:p.Pro110=
ENST00000696265.1:c.330G>A	ENSP00000512512.1:p.Pro110=
ENST00000696266.1:c.48G>A	ENSP00000512513.1:p.Pro16=
ENST00000229769.3:c.330G>A MANE Select	ENSP00000229769.2:p.Pro110=
ENST00000648059.1:c.330G>A	ENSP00000497902.1:p.Pro110=
ENST00000229769.2:c.330G>A	ENSP00000229769.2:p.Pro110=
NM_021922.2:c.330G>A , LRG_498t1:c.330G>A	NP_068741.1:p.Pro110=
XM_005248885.2:c.330G>A	XP_005248942.1:p.Pro110=
XM_005248886.2:c.330G>A	XP_005248943.1:p.Pro110=
XM_005248887.2:c.330G>A	XP_005248944.1:p.Pro110=
XM_005248888.2:c.330G>A	XP_005248945.1:p.Pro110=
XM_011514343.1:c.36G>A	XP_011512645.1:p.Pro12=
XM_011514344.1:c.36G>A	XP_011512646.1:p.Pro12=
XM_005248888.3:c.330G>A	XP_005248945.1:p.Pro110=
XM_011514343.2:c.36G>A	XP_011512645.1:p.Pro12=
XR_001743226.1:n.537G>A
XR_002956267.1:n.537G>A
NM_021922.3:c.330G>A MANE Select	NP_068741.1:p.Pro110=