Canonical Allele Identifier: CA2428355696

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688829_48688832delinsTCCA , CM000685.2:g.48688829_48688832delinsTCCA	GRCh38
NC_000023.10:g.48547218_48547221delinsTCCA , CM000685.1:g.48547218_48547221delinsTCCA	GRCh37
NC_000023.9:g.48432162_48432165delinsTCCA	NCBI36
NG_007877.1:g.10033_10036delinsTCCA , LRG_125:g.10033_10036delinsTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.345_348delinsTCCA
ENST00000698625.1:c.1101_1104delinsTCCA	ENSP00000513844.1:p.Pro367=
ENST00000698626.1:c.1101_1104delinsTCCA	ENSP00000513845.1:p.Pro367=
ENST00000698635.1:c.1101_1104delinsTCCA	ENSP00000513850.1:p.Pro367=
ENST00000376701.5:c.1101_1104delinsTCCA MANE Select	ENSP00000365891.4:p.Pro367=
ENST00000376701.4:c.1101_1104delinsTCCA	ENSP00000365891.4:p.Pro367=
ENST00000474174.1:n.345_348delinsTCCA
NM_000377.2:c.1101_1104delinsTCCA , LRG_125t1:c.1101_1104delinsTCCA	NP_000368.1:p.Pro367=
XM_011543977.1:c.945_948delinsTCCA	XP_011542279.1:p.Pro315=
XM_011543977.2:c.945_948delinsTCCA	XP_011542279.1:p.Pro315=
XM_017029786.1:c.1101_1104delinsTCCA	XP_016885275.1:p.Pro367=
NM_000377.3:c.1101_1104delinsTCCA MANE Select	NP_000368.1:p.Pro367=