Canonical Allele Identifier: CA413658058

Gene: SLC16A2

Linked Data

• COSMIC: COSM6432595
• MyVariant Identifiers: chrX:g.73745690A>T (hg19) ; chrX:g.74525855A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.74525855A>T , CM000685.2:g.74525855A>T	GRCh38
NC_000023.10:g.73745690A>T , CM000685.1:g.73745690A>T	GRCh37
NC_000023.9:g.73662415A>T	NCBI36
NG_011641.1:g.109606A>T
NG_011641.2:g.109606A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000587091.6:c.1132A>T MANE Select	ENSP00000465734.1:p.Ser378Cys
ENST00000636771.1:c.1041A>T
ENST00000587091.5:c.1132A>T	ENSP00000465734.1:p.Ser378Cys
ENST00000590447.1:c.572A>T
NM_006517.4:c.1132A>T	NP_006508.2:p.Ser378Cys
XM_005262294.1:c.1132A>T	XP_005262351.1:p.Ser378Cys
NM_006517.5:c.1132A>T MANE Select	NP_006508.2:p.Ser378Cys