Canonical Allele Identifier: CA208159727

Gene: SLC16A9

Linked Data

• dbSNP Id: rs966542444
• MyVariant Identifiers: chr10:g.61469034A>T (hg19) ; chr10:g.59709276A>T (hg38)

Genomic Alleles

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

Transcript Alleles

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