Canonical Allele Identifier: CA1913560945

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59654159T= , CM000672.2:g.59654159T=	GRCh38
NC_000010.10:g.61413917T= , CM000672.1:g.61413917T=	GRCh37
NC_000010.9:g.61083923T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.867A= MANE Select	ENSP00000378757.3:p.Leu289=
ENST00000395347.1:c.867A=	ENSP00000378756.1:p.Leu289=
ENST00000395348.7:c.867A=	ENSP00000378757.3:p.Leu289=
NM_194298.2:c.867A=	NP_919274.1:p.Leu289=
XM_011539488.1:c.867A=	XP_011537790.1:p.Leu289=
NM_001323977.1:c.606A=	NP_001310906.1:p.Leu202=
NM_001323978.1:c.606A=	NP_001310907.1:p.Leu202=
NM_001323979.1:c.606A=	NP_001310908.1:p.Leu202=
NM_001323980.1:c.606A=	NP_001310909.1:p.Leu202=
NM_001323981.1:c.867A=	NP_001310910.1:p.Leu289=
XM_017015883.1:c.867A=	XP_016871372.1:p.Leu289=
XM_017015884.2:c.867A=	XP_016871373.1:p.Leu289=
XM_024447878.1:c.867A=	XP_024303646.1:p.Leu289=
NM_001323978.2:c.606A=	NP_001310907.1:p.Leu202=
NM_001323979.2:c.606A=	NP_001310908.1:p.Leu202=
NM_001323980.2:c.606A=	NP_001310909.1:p.Leu202=
NM_001323981.2:c.867A=	NP_001310910.1:p.Leu289=
NM_194298.3:c.867A= MANE Select	NP_919274.1:p.Leu289=