Canonical Allele Identifier: CA243398

Gene: SLC16A2

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74524387G>A , CM000685.2:g.74524387G>A	GRCh38
NC_000023.10:g.73744222G>A , CM000685.1:g.73744222G>A	GRCh37
NC_000023.9:g.73660947G>A	NCBI36
NG_011641.1:g.108138G>A
NG_011641.2:g.108138G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006517.5:c.604G>A MANE Select	NP_006508.2:p.Gly202Arg
ENST00000587091.6:c.604G>A MANE Select	ENSP00000465734.1:p.Gly202Arg
NM_006517.4:c.604G>A	NP_006508.2:p.Gly202Arg
ENST00000587091.5:c.604G>A	ENSP00000465734.1:p.Gly202Arg
ENST00000590447.1:c.44G>A
ENST00000636771.1:c.513G>A
XM_005262294.1:c.604G>A	XP_005262351.1:p.Gly202Arg
XM_011531015.1:c.604G>A	XP_011529317.1:p.Gly202Arg