Canonical Allele Identifier: CA2740092134

Gene: WAS

Linked Data

• ClinVar Variation Id: 2922408
• ClinVar RCV Id: RCV003785622

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688472A>C , CM000685.2:g.48688472A>C	GRCh38
NC_000023.10:g.48546861A>C , CM000685.1:g.48546861A>C	GRCh37
NC_000023.9:g.48431805A>C	NCBI36
NG_007877.1:g.9676A>C , LRG_125:g.9676A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.175+19A>C
ENST00000698625.1:c.931+19A>C	ENSP00000513844.1:n.931+19A>C
ENST00000698626.1:c.931+19A>C	ENSP00000513845.1:n.931+19A>C
ENST00000698635.1:c.931+19A>C	ENSP00000513850.1:n.931+19A>C
ENST00000376701.5:c.931+19A>C MANE Select	ENSP00000365891.4:n.931+19A>C
ENST00000376701.4:c.931+19A>C	ENSP00000365891.4:n.931+19A>C
ENST00000474174.1:n.175+19A>C
NM_000377.2:c.931+19A>C , LRG_125t1:c.931+19A>C	NP_000368.1:n.931+19A>C
XM_011543977.1:c.931+19A>C	XP_011542279.1:n.931+19A>C
XM_011543977.2:c.931+19A>C	XP_011542279.1:n.931+19A>C
XM_017029786.1:c.931+19A>C	XP_016885275.1:n.931+19A>C
NM_000377.3:c.931+19A>C MANE Select	NP_000368.1:n.931+19A>C