Canonical Allele Identifier: CA412873283
Gene: WAS HGNC NCBI

Linked Data

gnomAD v4: X-48688825-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.48688825G>C , CM000685.2:g.48688825G>C GRCh38
NC_000023.10:g.48547214G>C , CM000685.1:g.48547214G>C GRCh37
NC_000023.9:g.48432158G>C NCBI36
NG_007877.1:g.10029G>C , LRG_125:g.10029G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000474174.2:n.341G>C
ENST00000698625.1:c.1097G>C ENSP00000513844.1:p.Gly366Ala
ENST00000698626.1:c.1097G>C ENSP00000513845.1:p.Gly366Ala
ENST00000698635.1:c.1097G>C ENSP00000513850.1:p.Gly366Ala
ENST00000376701.5:c.1097G>C MANE Select ENSP00000365891.4:p.Gly366Ala
ENST00000376701.4:c.1097G>C ENSP00000365891.4:p.Gly366Ala
ENST00000474174.1:n.341G>C
NM_000377.2:c.1097G>C , LRG_125t1:c.1097G>C NP_000368.1:p.Gly366Ala
XM_011543977.1:c.941G>C XP_011542279.1:p.Gly314Ala
XM_011543977.2:c.941G>C XP_011542279.1:p.Gly314Ala
XM_017029786.1:c.1097G>C XP_016885275.1:p.Gly366Ala
NM_000377.3:c.1097G>C MANE Select NP_000368.1:p.Gly366Ala