Canonical Allele Identifier: CA1913561206

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59654259T= , CM000672.2:g.59654259T=	GRCh38
NC_000010.10:g.61414017T= , CM000672.1:g.61414017T=	GRCh37
NC_000010.9:g.61084023T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.767A= MANE Select	ENSP00000378757.3:p.Asn256=
ENST00000395347.1:c.767A=	ENSP00000378756.1:p.Asn256=
ENST00000395348.7:c.767A=	ENSP00000378757.3:p.Asn256=
NM_194298.2:c.767A=	NP_919274.1:p.Asn256=
XM_011539488.1:c.767A=	XP_011537790.1:p.Asn256=
NM_001323977.1:c.506A=	NP_001310906.1:p.Asn169=
NM_001323978.1:c.506A=	NP_001310907.1:p.Asn169=
NM_001323979.1:c.506A=	NP_001310908.1:p.Asn169=
NM_001323980.1:c.506A=	NP_001310909.1:p.Asn169=
NM_001323981.1:c.767A=	NP_001310910.1:p.Asn256=
XM_017015883.1:c.767A=	XP_016871372.1:p.Asn256=
XM_017015884.2:c.767A=	XP_016871373.1:p.Asn256=
XM_024447878.1:c.767A=	XP_024303646.1:p.Asn256=
NM_001323978.2:c.506A=	NP_001310907.1:p.Asn169=
NM_001323979.2:c.506A=	NP_001310908.1:p.Asn169=
NM_001323980.2:c.506A=	NP_001310909.1:p.Asn169=
NM_001323981.2:c.767A=	NP_001310910.1:p.Asn256=
NM_194298.3:c.767A= MANE Select	NP_919274.1:p.Asn256=