Canonical Allele Identifier: CA413655917

Gene: SLC16A2

Linked Data

• gnomAD v4: X-74421804-A-G
• MyVariant Identifiers: chrX:g.73641639A>G (hg19) ; chrX:g.74421804A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421804A>G , CM000685.2:g.74421804A>G	GRCh38
NC_000023.10:g.73641639A>G , CM000685.1:g.73641639A>G	GRCh37
NC_000023.9:g.73558364A>G	NCBI36
NG_011641.1:g.5555A>G
NG_011641.2:g.5555A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.167A>G MANE Select	ENSP00000465734.1:p.Gln56Arg
ENST00000587091.5:c.167A>G	ENSP00000465734.1:p.Gln56Arg
NM_006517.4:c.167A>G	NP_006508.2:p.Gln56Arg
XM_005262294.1:c.167A>G	XP_005262351.1:p.Gln56Arg
XM_011531015.1:c.167A>G	XP_011529317.1:p.Gln56Arg
NM_006517.5:c.167A>G MANE Select	NP_006508.2:p.Gln56Arg