Canonical Allele Identifier: CA10403989

Gene: WAS

Linked Data

• ClinVar Variation Id: 2938981
• ClinVar RCV Id: RCV003791707
• dbSNP Id: rs782381708
• ExAC: X:48546675 T / C
• gnomAD v2: X-48546675-T-C
• gnomAD v3: X-48688286-T-C
• gnomAD v4: X-48688286-T-C
• MyVariant Identifiers: chrX:g.48546675T>C (hg19) ; chrX:g.48688286T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688286T>C , CM000685.2:g.48688286T>C	GRCh38
NC_000023.10:g.48546675T>C , CM000685.1:g.48546675T>C	GRCh37
NC_000023.9:g.48431619T>C	NCBI36
NG_007877.1:g.9490T>C , LRG_125:g.9490T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.8T>C
ENST00000483750.6:n.1000T>C
ENST00000698625.1:c.778-14T>C	ENSP00000513844.1:n.778-14T>C
ENST00000698626.1:c.778-14T>C	ENSP00000513845.1:n.778-14T>C
ENST00000698635.1:c.778-14T>C	ENSP00000513850.1:n.778-14T>C
ENST00000376701.5:c.778-14T>C MANE Select	ENSP00000365891.4:n.778-14T>C
ENST00000376701.4:c.778-14T>C	ENSP00000365891.4:n.778-14T>C
ENST00000474174.1:n.8T>C
NM_000377.2:c.778-14T>C , LRG_125t1:c.778-14T>C	NP_000368.1:n.778-14T>C
XM_011543977.1:c.778-14T>C	XP_011542279.1:n.778-14T>C
XM_011543977.2:c.778-14T>C	XP_011542279.1:n.778-14T>C
XM_017029786.1:c.778-14T>C	XP_016885275.1:n.778-14T>C
NM_000377.3:c.778-14T>C MANE Select	NP_000368.1:n.778-14T>C