Canonical Allele Identifier: CA1132960971

Gene: WAS

Linked Data

• dbSNP Id: rs2062426136
• gnomAD v3: X-48688225-CAACGACAATCCAT-C
• gnomAD v4: X-48688225-CAACGACAATCCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688226_48688238del , CM000685.2:g.48688226_48688238del	GRCh38
NC_000023.10:g.48546615_48546627del , CM000685.1:g.48546615_48546627del	GRCh37
NC_000023.9:g.48431559_48431571del	NCBI36
NG_007877.1:g.9430_9442del , LRG_125:g.9430_9442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000483750.6:n.940_952del
ENST00000698625.1:c.778-74_778-62del	ENSP00000513844.1:n.778-74_778-62del
ENST00000698626.1:c.778-74_778-62del	ENSP00000513845.1:n.778-74_778-62del
ENST00000698635.1:c.778-74_778-62del	ENSP00000513850.1:n.778-74_778-62del
ENST00000376701.5:c.778-74_778-62del MANE Select	ENSP00000365891.4:n.778-74_778-62del
ENST00000376701.4:c.778-74_778-62del	ENSP00000365891.4:n.778-74_778-62del
NM_000377.2:c.778-74_778-62del , LRG_125t1:c.778-74_778-62del	NP_000368.1:n.778-74_778-62del
XM_011543977.1:c.778-74_778-62del	XP_011542279.1:n.778-74_778-62del
XM_011543977.2:c.778-74_778-62del	XP_011542279.1:n.778-74_778-62del
XM_017029786.1:c.778-74_778-62del	XP_016885275.1:n.778-74_778-62del
NM_000377.3:c.778-74_778-62del MANE Select	NP_000368.1:n.778-74_778-62del