Canonical Allele Identifier: CA413658203

Gene: SLC16A2

Linked Data

• MyVariant Identifiers: chrX:g.73749069G>T (hg19) ; chrX:g.74529234G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74529234G>T , CM000685.2:g.74529234G>T	GRCh38
NC_000023.10:g.73749069G>T , CM000685.1:g.73749069G>T	GRCh37
NC_000023.9:g.73665794G>T	NCBI36
NG_011641.1:g.112985G>T
NG_011641.2:g.112985G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.1192G>T MANE Select	ENSP00000465734.1:p.Gly398Cys
ENST00000636771.1:c.1101G>T
ENST00000587091.5:c.1192G>T	ENSP00000465734.1:p.Gly398Cys
ENST00000590447.1:c.611-2099G>T
NM_006517.4:c.1192G>T	NP_006508.2:p.Gly398Cys
XM_005262294.1:c.1171-2099G>T	XP_005262351.1:n.1171-2099G>T
NM_006517.5:c.1192G>T MANE Select	NP_006508.2:p.Gly398Cys