Canonical Allele Identifier: CA5595625

Gene: SLC16A12 SLC16A12-AS1

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_213606.4:c.49T>G (SLC16A12) MANE Select	NP_998771.3:p.Trp17Gly
ENST00000371790.5:c.49T>G (SLC16A12) MANE Select	ENSP00000360855.4:p.Trp17Gly
NM_213606.3:c.49T>G (SLC16A12)	NP_998771.3:p.Trp17Gly
NR_120614.1:n.274A>C (SLC16A12-AS1)
ENST00000371790.4:c.49T>G (SLC16A12)	ENSP00000360855.4:p.Trp17Gly
ENST00000475682.1:c.49T>G (SLC16A12)	ENSP00000436965.1:p.Trp17Gly
XM_017016237.2:c.49T>G (SLC16A12)	XP_016871726.1:p.Trp17Gly
XM_017016238.1:c.49T>G (SLC16A12)	XP_016871727.1:p.Trp17Gly
XM_017016239.1:c.49T>G (SLC16A12)	XP_016871728.1:p.Trp17Gly
XM_024447994.1:c.49T>G (SLC16A12)	XP_024303762.1:p.Trp17Gly