Canonical Allele Identifier: CA370917210

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30925841A>T (hg19) ; chr8:g.31068325A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068325A>T , CM000670.2:g.31068325A>T	GRCh38
NC_000008.10:g.30925841A>T , CM000670.1:g.30925841A>T	GRCh37
NC_000008.9:g.31045383A>T	NCBI36
NG_008870.1:g.40064A>T , LRG_524:g.40064A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.722A>T MANE Select	ENSP00000298139.5:p.Lys241Ile
ENST00000650667.1:c.*336A>T	ENSP00000498593.1:n.*336A>T
ENST00000651642.1:c.17A>T	ENSP00000498779.1:p.Lys6Ile
ENST00000298139.5:c.722A>T	ENSP00000298139.5:p.Lys241Ile
NM_000553.4:c.722A>T , LRG_524t1:c.722A>T	NP_000544.2:p.Lys241Ile
XM_011544639.1:c.722A>T	XP_011542941.1:p.Lys241Ile
XR_949470.1:n.995A>T
XR_949471.1:n.995A>T
XR_949472.1:n.995A>T
NM_000553.5:c.722A>T	NP_000544.2:p.Lys241Ile
XM_011544639.3:c.722A>T	XP_011542941.1:p.Lys241Ile
XM_024447265.1:c.512A>T	XP_024303033.1:p.Lys171Ile
XR_949470.3:n.1023A>T
XR_949471.3:n.1023A>T
XR_949472.3:n.1023A>T
NM_000553.6:c.722A>T MANE Select	NP_000544.2:p.Lys241Ile