Canonical Allele Identifier: CA370915363

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30977819A>C (hg19) ; chr8:g.31120303A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120303A>C , CM000670.2:g.31120303A>C	GRCh38
NC_000008.10:g.30977819A>C , CM000670.1:g.30977819A>C	GRCh37
NC_000008.9:g.31097361A>C	NCBI36
NG_008870.1:g.92042A>C , LRG_524:g.92042A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.2509A>C MANE Select	ENSP00000298139.5:p.Ile837Leu
ENST00000650667.1:c.*2123A>C	ENSP00000498593.1:n.*2123A>C
ENST00000298139.5:c.2509A>C	ENSP00000298139.5:p.Ile837Leu
ENST00000520169.1:n.348A>C
ENST00000521620.5:n.1142A>C
NM_000553.4:c.2509A>C , LRG_524t1:c.2509A>C	NP_000544.2:p.Ile837Leu
XM_011544639.1:c.2428A>C	XP_011542941.1:p.Ile810Leu
XM_011544640.1:c.910A>C	XP_011542942.1:p.Ile304Leu
XR_949470.1:n.2782A>C
XR_949471.1:n.2782A>C
XR_949472.1:n.2782A>C
NM_000553.5:c.2509A>C	NP_000544.2:p.Ile837Leu
XM_011544639.3:c.2428A>C	XP_011542941.1:p.Ile810Leu
XM_024447265.1:c.2299A>C	XP_024303033.1:p.Ile767Leu
XR_949470.3:n.2810A>C
XR_949471.3:n.2810A>C
XR_949472.3:n.2810A>C
NM_000553.6:c.2509A>C MANE Select	NP_000544.2:p.Ile837Leu