Canonical Allele Identifier: CA370921027
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31081188G>C , CM000670.2:g.31081188G>C GRCh38
NC_000008.10:g.30938704G>C , CM000670.1:g.30938704G>C GRCh37
NC_000008.9:g.31058246G>C NCBI36
NG_008870.1:g.52927G>C , LRG_524:g.52927G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.1161G>C MANE Select ENSP00000298139.5:p.Met387Ile
ENST00000650667.1:c.*775G>C ENSP00000498593.1:n.*775G>C
ENST00000651642.1:c.456G>C ENSP00000498779.1:p.Met152Ile
ENST00000298139.5:c.1161G>C ENSP00000298139.5:p.Met387Ile
NM_000553.4:c.1161G>C , LRG_524t1:c.1161G>C NP_000544.2:p.Met387Ile
XM_011544639.1:c.1161G>C XP_011542941.1:p.Met387Ile
XR_949470.1:n.1434G>C
XR_949471.1:n.1434G>C
XR_949472.1:n.1434G>C
NM_000553.5:c.1161G>C NP_000544.2:p.Met387Ile
XM_011544639.3:c.1161G>C XP_011542941.1:p.Met387Ile
XM_024447265.1:c.951G>C XP_024303033.1:p.Met317Ile
XR_949470.3:n.1462G>C
XR_949471.3:n.1462G>C
XR_949472.3:n.1462G>C
NM_000553.6:c.1161G>C MANE Select NP_000544.2:p.Met387Ile