Canonical Allele Identifier: CA370925430

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31004619T>G (hg19) ; chr8:g.31147103T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147103T>G , CM000670.2:g.31147103T>G	GRCh38
NC_000008.10:g.31004619T>G , CM000670.1:g.31004619T>G	GRCh37
NC_000008.9:g.31124161T>G	NCBI36
NG_008870.1:g.118842T>G , LRG_524:g.118842T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3434T>G MANE Select	ENSP00000298139.5:p.Ile1145Ser
ENST00000650667.1:c.*3048T>G	ENSP00000498593.1:n.*3048T>G
ENST00000298139.5:c.3434T>G	ENSP00000298139.5:p.Ile1145Ser
ENST00000521620.5:n.2067T>G
NM_000553.4:c.3434T>G , LRG_524t1:c.3434T>G	NP_000544.2:p.Ile1145Ser
XM_011544639.1:c.3353T>G	XP_011542941.1:p.Ile1118Ser
XM_011544640.1:c.1835T>G	XP_011542942.1:p.Ile612Ser
XR_949470.1:n.3707T>G
XR_949471.1:n.3707T>G
XR_949472.1:n.3707T>G
XR_949643.1:n.614+1405A>C
NM_000553.5:c.3434T>G	NP_000544.2:p.Ile1145Ser
XM_011544639.3:c.3353T>G	XP_011542941.1:p.Ile1118Ser
XM_024447265.1:c.3224T>G	XP_024303033.1:p.Ile1075Ser
XR_949470.3:n.3735T>G
XR_949471.3:n.3735T>G
XR_949472.3:n.3735T>G
NM_000553.6:c.3434T>G MANE Select	NP_000544.2:p.Ile1145Ser