Canonical Allele Identifier: CA370911715

Gene: WRN

Linked Data

• gnomAD v4: 8-31173044-G-C
• MyVariant Identifiers: chr8:g.31030560G>C (hg19) ; chr8:g.31173044G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173044G>C , CM000670.2:g.31173044G>C	GRCh38
NC_000008.10:g.31030560G>C , CM000670.1:g.31030560G>C	GRCh37
NC_000008.9:g.31150102G>C	NCBI36
NG_008870.1:g.144783G>C , LRG_524:g.144783G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4241G>C MANE Select	ENSP00000298139.5:p.Gly1414Ala
ENST00000650667.1:c.*3855G>C	ENSP00000498593.1:n.*3855G>C
ENST00000651946.1:n.465G>C
ENST00000298139.5:c.4241G>C	ENSP00000298139.5:p.Gly1414Ala
ENST00000521620.5:n.2874G>C
NM_000553.4:c.4241G>C , LRG_524t1:c.4241G>C	NP_000544.2:p.Gly1414Ala
XM_011544639.1:c.4160G>C	XP_011542941.1:p.Gly1387Ala
XM_011544640.1:c.2642G>C	XP_011542942.1:p.Gly881Ala
XR_949643.1:n.88-1726C>G
XR_949644.1:n.88-1726C>G
XR_949645.1:n.88-1726C>G
XR_949646.1:n.88-1726C>G
XR_949647.1:n.701-1726C>G
XR_949648.1:n.603-1726C>G
NM_000553.5:c.4241G>C	NP_000544.2:p.Gly1414Ala
XM_011544639.3:c.4160G>C	XP_011542941.1:p.Gly1387Ala
XM_024447265.1:c.4031G>C	XP_024303033.1:p.Gly1344Ala
NM_000553.6:c.4241G>C MANE Select	NP_000544.2:p.Gly1414Ala