Canonical Allele Identifier: CA370916212

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924640A>C (hg19) ; chr8:g.31067124A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067124A>C , CM000670.2:g.31067124A>C	GRCh38
NC_000008.10:g.30924640A>C , CM000670.1:g.30924640A>C	GRCh37
NC_000008.9:g.31044182A>C	NCBI36
NG_008870.1:g.38863A>C , LRG_524:g.38863A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.596A>C MANE Select	ENSP00000298139.5:p.Asn199Thr
ENST00000650667.1:c.*210A>C	ENSP00000498593.1:n.*210A>C
ENST00000298139.5:c.596A>C	ENSP00000298139.5:p.Asn199Thr
NM_000553.4:c.596A>C , LRG_524t1:c.596A>C	NP_000544.2:p.Asn199Thr
XM_011544639.1:c.596A>C	XP_011542941.1:p.Asn199Thr
XR_949470.1:n.869A>C
XR_949471.1:n.869A>C
XR_949472.1:n.869A>C
NM_000553.5:c.596A>C	NP_000544.2:p.Asn199Thr
XM_011544639.3:c.596A>C	XP_011542941.1:p.Asn199Thr
XM_024447265.1:c.386A>C	XP_024303033.1:p.Asn129Thr
XR_949470.3:n.897A>C
XR_949471.3:n.897A>C
XR_949472.3:n.897A>C
NM_000553.6:c.596A>C MANE Select	NP_000544.2:p.Asn199Thr