Canonical Allele Identifier: CA137294644

Gene: FANCE

Linked Data

• ClinVar Variation Id: 1524207
• ClinVar RCV Id: RCV002031550
• dbSNP Id: rs1016962570
• gnomAD v4: 6-35455959-C-T
• MyVariant Identifiers: chr6:g.35423736C>T (hg19) ; chr6:g.35455959C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.35455959C>T , CM000668.2:g.35455959C>T	GRCh38
NC_000006.11:g.35423736C>T , CM000668.1:g.35423736C>T	GRCh37
NC_000006.10:g.35531714C>T	NCBI36
NG_011708.1:g.8599C>T , LRG_498:g.8599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696264.1:c.461C>T	ENSP00000512511.1:p.Ser154Phe
ENST00000696265.1:c.461C>T	ENSP00000512512.1:p.Ser154Phe
ENST00000696266.1:c.179C>T	ENSP00000512513.1:p.Ser60Phe
ENST00000696267.1:n.101C>T
ENST00000229769.3:c.461C>T MANE Select	ENSP00000229769.2:p.Ser154Phe
ENST00000648059.1:c.461C>T	ENSP00000497902.1:p.Ser154Phe
ENST00000229769.2:c.461C>T	ENSP00000229769.2:p.Ser154Phe
NM_021922.2:c.461C>T , LRG_498t1:c.461C>T	NP_068741.1:p.Ser154Phe
XM_005248885.2:c.461C>T	XP_005248942.1:p.Ser154Phe
XM_005248886.2:c.461C>T	XP_005248943.1:p.Ser154Phe
XM_005248887.2:c.461C>T	XP_005248944.1:p.Ser154Phe
XM_005248888.2:c.461C>T	XP_005248945.1:p.Ser154Phe
XM_011514343.1:c.167C>T	XP_011512645.1:p.Ser56Phe
XM_011514344.1:c.167C>T	XP_011512646.1:p.Ser56Phe
XM_005248888.3:c.461C>T	XP_005248945.1:p.Ser154Phe
XM_011514343.2:c.167C>T	XP_011512645.1:p.Ser56Phe
XR_001743226.1:n.668C>T
XR_002956267.1:n.668C>T
NM_021922.3:c.461C>T MANE Select	NP_068741.1:p.Ser154Phe