Canonical Allele Identifier: CA1913559165

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59653595A= , CM000672.2:g.59653595A=	GRCh38
NC_000010.10:g.61413353A= , CM000672.1:g.61413353A=	GRCh37
NC_000010.9:g.61083359A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_194298.3:c.1351+80T= MANE Select	NP_919274.1:n.1351+80T=
ENST00000395348.8:c.1351+80T= MANE Select	ENSP00000378757.3:n.1351+80T=
NM_001323977.1:c.1090+80T=	NP_001310906.1:n.1090+80T=
NM_001323978.1:c.1090+80T=	NP_001310907.1:n.1090+80T=
NM_001323978.2:c.1090+80T=	NP_001310907.1:n.1090+80T=
NM_001323979.1:c.1090+80T=	NP_001310908.1:n.1090+80T=
NM_001323979.2:c.1090+80T=	NP_001310908.1:n.1090+80T=
NM_001323980.1:c.1090+80T=	NP_001310909.1:n.1090+80T=
NM_001323980.2:c.1090+80T=	NP_001310909.1:n.1090+80T=
NM_001323981.1:c.1351+80T=	NP_001310910.1:n.1351+80T=
NM_001323981.2:c.1351+80T=	NP_001310910.1:n.1351+80T=
NM_194298.2:c.1351+80T=	NP_919274.1:n.1351+80T=
ENST00000395347.1:c.1351+80T=	ENSP00000378756.1:n.1351+80T=
ENST00000395348.7:c.1351+80T=	ENSP00000378757.3:n.1351+80T=
XM_011539488.1:c.1351+80T=	XP_011537790.1:n.1351+80T=
XM_017015883.1:c.1431T=	XP_016871372.1:p.Asn477=
XM_017015884.2:c.1351+80T=	XP_016871373.1:n.1351+80T=
XM_024447878.1:c.1351+80T=	XP_024303646.1:n.1351+80T=