Canonical Allele Identifier: CA1913587708

Gene: SLC16A9

Linked Data

• dbSNP Id: rs899540932

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709342A>T , CM000672.2:g.59709342A>T	GRCh38
NC_000010.10:g.61469100A>T , CM000672.1:g.61469100A>T	GRCh37
NC_000010.9:g.61139106A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.-37+137T>A MANE Select	ENSP00000378757.3:n.-37+137T>A
ENST00000395347.1:c.-36-25015T>A	ENSP00000378756.1:n.-36-25015T>A
ENST00000395348.7:c.-37+137T>A	ENSP00000378757.3:n.-37+137T>A
ENST00000490066.1:n.44+137T>A
NM_194298.2:c.-37+137T>A	NP_919274.1:n.-37+137T>A
NM_001323977.1:c.-168+670T>A	NP_001310906.1:n.-168+670T>A
NM_001323978.1:c.-251+137T>A	NP_001310907.1:n.-251+137T>A
NM_001323979.1:c.-168+367T>A	NP_001310908.1:n.-168+367T>A
NM_001323980.1:c.-168+137T>A	NP_001310909.1:n.-168+137T>A
NM_001323981.1:c.-120+137T>A	NP_001310910.1:n.-120+137T>A
XM_017015883.1:c.-37+137T>A	XP_016871372.1:n.-37+137T>A
XM_017015884.2:c.-182+137T>A	XP_016871373.1:n.-182+137T>A
NM_001323978.2:c.-251+137T>A	NP_001310907.1:n.-251+137T>A
NM_001323979.2:c.-168+367T>A	NP_001310908.1:n.-168+367T>A
NM_001323980.2:c.-168+137T>A	NP_001310909.1:n.-168+137T>A
NM_001323981.2:c.-120+137T>A	NP_001310910.1:n.-120+137T>A
NM_194298.3:c.-37+137T>A MANE Select	NP_919274.1:n.-37+137T>A