Canonical Allele Identifier: CA517464284

Gene: SLC16A2

Linked Data

• MyVariant Identifiers: chrX:g.73641619C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74421784C>T , CM000685.2:g.74421784C>T	GRCh38
NC_000023.10:g.73641619C>T , CM000685.1:g.73641619C>T	GRCh37
NC_000023.9:g.73558344C>T	NCBI36
NG_011641.1:g.5535C>T
NG_011641.2:g.5535C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587091.6:c.147C>T MANE Select	ENSP00000465734.1:p.Pro49=
ENST00000587091.5:c.147C>T	ENSP00000465734.1:p.Pro49=
NM_006517.4:c.147C>T	NP_006508.2:p.Pro49=
XM_005262294.1:c.147C>T	XP_005262351.1:p.Pro49=
XM_011531015.1:c.147C>T	XP_011529317.1:p.Pro49=
NM_006517.5:c.147C>T MANE Select	NP_006508.2:p.Pro49=