Canonical Allele Identifier: CA370911835

Gene: WRN

Linked Data

• gnomAD v4: 8-31173070-G-T
• MyVariant Identifiers: chr8:g.31030586G>T (hg19) ; chr8:g.31173070G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173070G>T , CM000670.2:g.31173070G>T	GRCh38
NC_000008.10:g.31030586G>T , CM000670.1:g.31030586G>T	GRCh37
NC_000008.9:g.31150128G>T	NCBI36
NG_008870.1:g.144809G>T , LRG_524:g.144809G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4267G>T MANE Select	ENSP00000298139.5:p.Asp1423Tyr
ENST00000650667.1:c.*3881G>T	ENSP00000498593.1:n.*3881G>T
ENST00000651946.1:n.491G>T
ENST00000298139.5:c.4267G>T	ENSP00000298139.5:p.Asp1423Tyr
ENST00000521620.5:n.2900G>T
NM_000553.4:c.4267G>T , LRG_524t1:c.4267G>T	NP_000544.2:p.Asp1423Tyr
XM_011544639.1:c.4186G>T	XP_011542941.1:p.Asp1396Tyr
XM_011544640.1:c.2668G>T	XP_011542942.1:p.Asp890Tyr
XR_949643.1:n.88-1752C>A
XR_949644.1:n.88-1752C>A
XR_949645.1:n.88-1752C>A
XR_949646.1:n.88-1752C>A
XR_949647.1:n.701-1752C>A
XR_949648.1:n.603-1752C>A
NM_000553.5:c.4267G>T	NP_000544.2:p.Asp1423Tyr
XM_011544639.3:c.4186G>T	XP_011542941.1:p.Asp1396Tyr
XM_024447265.1:c.4057G>T	XP_024303033.1:p.Asp1353Tyr
NM_000553.6:c.4267G>T MANE Select	NP_000544.2:p.Asp1423Tyr