Canonical Allele Identifier: CA370928209

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31090935C>T , CM000670.2:g.31090935C>T	GRCh38
NC_000008.10:g.30948451C>T , CM000670.1:g.30948451C>T	GRCh37
NC_000008.9:g.31067993C>T	NCBI36
NG_008870.1:g.62674C>T , LRG_524:g.62674C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1822C>T MANE Select	NP_000544.2:p.Gln608Ter
ENST00000298139.7:c.1822C>T MANE Select	ENSP00000298139.5:p.Gln608Ter
NM_000553.4:c.1822C>T , LRG_524t1:c.1822C>T	NP_000544.2:p.Gln608Ter
NM_000553.5:c.1822C>T	NP_000544.2:p.Gln608Ter
ENST00000298139.5:c.1822C>T	ENSP00000298139.5:p.Gln608Ter
ENST00000521620.5:n.455C>T
ENST00000650667.1:c.*1436C>T	ENSP00000498593.1:n.*1436C>T
XM_011544639.1:c.1741C>T	XP_011542941.1:p.Gln581Ter
XM_011544639.3:c.1741C>T	XP_011542941.1:p.Gln581Ter
XM_011544640.1:c.223C>T	XP_011542942.1:p.Gln75Ter
XM_024447265.1:c.1612C>T	XP_024303033.1:p.Gln538Ter
XR_949470.1:n.2095C>T
XR_949470.3:n.2123C>T
XR_949471.1:n.2095C>T
XR_949471.3:n.2123C>T
XR_949472.1:n.2095C>T
XR_949472.3:n.2123C>T