Canonical Allele Identifier: CA1926838192

Gene: SLC16A12 SLC16A12-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89462530A= , CM000672.2:g.89462530A=	GRCh38
NC_000010.10:g.91222287A= , CM000672.1:g.91222287A=	GRCh37
NC_000010.9:g.91212267A=	NCBI36
NG_021179.1:g.78027T=

Transcript Alleles

HGVS	Amino-acid Change
NM_213606.4:c.49T= (SLC16A12) MANE Select	NP_998771.3:p.Trp17=
ENST00000371790.5:c.49T= (SLC16A12) MANE Select	ENSP00000360855.4:p.Trp17=
NM_213606.3:c.49T= (SLC16A12)	NP_998771.3:p.Trp17=
NR_120614.1:n.274A= (SLC16A12-AS1)
ENST00000371790.4:c.49T= (SLC16A12)	ENSP00000360855.4:p.Trp17=
ENST00000475682.1:c.49T= (SLC16A12)	ENSP00000436965.1:p.Trp17=
XM_017016237.2:c.49T= (SLC16A12)	XP_016871726.1:p.Trp17=
XM_017016238.1:c.49T= (SLC16A12)	XP_016871727.1:p.Trp17=
XM_017016239.1:c.49T= (SLC16A12)	XP_016871728.1:p.Trp17=
XM_024447994.1:c.49T= (SLC16A12)	XP_024303762.1:p.Trp17=