Canonical Allele Identifier: CA1913586831

Gene: SLC16A9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707424G= , CM000672.2:g.59707424G=	GRCh38
NC_000010.10:g.61467182G= , CM000672.1:g.61467182G=	GRCh37
NC_000010.9:g.61137188G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+2055C= MANE Select	ENSP00000378757.3:n.-37+2055C=
ENST00000395347.1:c.-36-23097C=	ENSP00000378756.1:n.-36-23097C=
ENST00000395348.7:c.-37+2055C=	ENSP00000378757.3:n.-37+2055C=
ENST00000490066.1:n.222+1182C=
NM_194298.2:c.-37+2055C=	NP_919274.1:n.-37+2055C=
NM_001323977.1:c.-168+2588C=	NP_001310906.1:n.-168+2588C=
NM_001323978.1:c.-250-236C=	NP_001310907.1:n.-250-236C=
NM_001323979.1:c.-168+2285C=	NP_001310908.1:n.-168+2285C=
NM_001323980.1:c.-168+2055C=	NP_001310909.1:n.-168+2055C=
NM_001323981.1:c.-119-236C=	NP_001310910.1:n.-119-236C=
XM_017015883.1:c.-37+2055C=	XP_016871372.1:n.-37+2055C=
XM_017015884.2:c.-182+2055C=	XP_016871373.1:n.-182+2055C=
NM_001323978.2:c.-250-236C=	NP_001310907.1:n.-250-236C=
NM_001323979.2:c.-168+2285C=	NP_001310908.1:n.-168+2285C=
NM_001323980.2:c.-168+2055C=	NP_001310909.1:n.-168+2055C=
NM_001323981.2:c.-119-236C=	NP_001310910.1:n.-119-236C=
NM_194298.3:c.-37+2055C= MANE Select	NP_919274.1:n.-37+2055C=