Canonical Allele Identifier: CA1913587677

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709276A= , CM000672.2:g.59709276A=	GRCh38
NC_000010.10:g.61469034A= , CM000672.1:g.61469034A=	GRCh37
NC_000010.9:g.61139040A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+203T= MANE Select	ENSP00000378757.3:n.-37+203T=
ENST00000395347.1:c.-36-24949T=	ENSP00000378756.1:n.-36-24949T=
ENST00000395348.7:c.-37+203T=	ENSP00000378757.3:n.-37+203T=
ENST00000490066.1:n.44+203T=
NM_194298.2:c.-37+203T=	NP_919274.1:n.-37+203T=
NM_001323977.1:c.-168+736T=	NP_001310906.1:n.-168+736T=
NM_001323978.1:c.-251+203T=	NP_001310907.1:n.-251+203T=
NM_001323979.1:c.-168+433T=	NP_001310908.1:n.-168+433T=
NM_001323980.1:c.-168+203T=	NP_001310909.1:n.-168+203T=
NM_001323981.1:c.-120+203T=	NP_001310910.1:n.-120+203T=
XM_017015883.1:c.-37+203T=	XP_016871372.1:n.-37+203T=
XM_017015884.2:c.-182+203T=	XP_016871373.1:n.-182+203T=
NM_001323978.2:c.-251+203T=	NP_001310907.1:n.-251+203T=
NM_001323979.2:c.-168+433T=	NP_001310908.1:n.-168+433T=
NM_001323980.2:c.-168+203T=	NP_001310909.1:n.-168+203T=
NM_001323981.2:c.-120+203T=	NP_001310910.1:n.-120+203T=
NM_194298.3:c.-37+203T= MANE Select	NP_919274.1:n.-37+203T=