Canonical Allele Identifier: CA517241114
Gene: SLC16A2 HGNC NCBI

Linked Data

gnomAD v4: X-74525761-G-A
MyVariant Identifiers: chrX:g.73745596G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525761G>A , CM000685.2:g.74525761G>A GRCh38
NC_000023.10:g.73745596G>A , CM000685.1:g.73745596G>A GRCh37
NC_000023.9:g.73662321G>A NCBI36
NG_011641.1:g.109512G>A
NG_011641.2:g.109512G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1038G>A MANE Select ENSP00000465734.1:p.Val346=
ENST00000636771.1:c.947G>A
ENST00000587091.5:c.1038G>A ENSP00000465734.1:p.Val346=
ENST00000590447.1:c.478G>A
NM_006517.4:c.1038G>A NP_006508.2:p.Val346=
XM_005262294.1:c.1038G>A XP_005262351.1:p.Val346=
XM_011531015.1:c.*42G>A XP_011529317.1:n.*42G>A
NM_006517.5:c.1038G>A MANE Select NP_006508.2:p.Val346=