Canonical Allele Identifier: CA658179158

Gene: WAS

Linked Data

• COSMIC: COSN24982308

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48689165_48689166insACACC , CM000685.2:g.48689165_48689166insACACC	GRCh38
NC_000023.10:g.48547554_48547555insACACC , CM000685.1:g.48547554_48547555insACACC	GRCh37
NC_000023.9:g.48432498_48432499insACACC	NCBI36
NG_007877.1:g.10369_10370insACACC , LRG_125:g.10369_10370insACACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.582+99_582+100insACACC
ENST00000698625.1:c.1338+99_1338+100insACACC	ENSP00000513844.1:n.1338+99_1338+100insACACC
ENST00000698626.1:c.1338+99_1338+100insACACC	ENSP00000513845.1:n.1338+99_1338+100insACACC
ENST00000698635.1:c.1338+99_1338+100insACACC	ENSP00000513850.1:n.1338+99_1338+100insACACC
ENST00000376701.5:c.1338+99_1338+100insACACC MANE Select	ENSP00000365891.4:n.1338+99_1338+100insACACC
ENST00000376701.4:c.1338+99_1338+100insACACC	ENSP00000365891.4:n.1338+99_1338+100insACACC
ENST00000470107.1:n.47+99_47+100insACACC
NM_000377.2:c.1338+99_1338+100insACACC , LRG_125t1:c.1338+99_1338+100insACACC	NP_000368.1:n.1338+99_1338+100insACACC
XM_011543977.1:c.1182+99_1182+100insACACC	XP_011542279.1:n.1182+99_1182+100insACACC
XM_011543977.2:c.1182+99_1182+100insACACC	XP_011542279.1:n.1182+99_1182+100insACACC
XM_017029786.1:c.1338+99_1338+100insACACC	XP_016885275.1:n.1338+99_1338+100insACACC
NM_000377.3:c.1338+99_1338+100insACACC MANE Select	NP_000368.1:n.1338+99_1338+100insACACC