Canonical Allele Identifier: CA928948227

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1171614
• gnomAD v3: 10-59709780-T-A
• gnomAD v4: 10-59709780-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709780T>A , CM000672.2:g.59709780T>A	GRCh38
NC_000010.10:g.61469538T>A , CM000672.1:g.61469538T>A	GRCh37
NC_000010.9:g.61139544T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.-338A>T MANE Select	ENSP00000378757.3:n.-338A>T
ENST00000395347.1:c.-36-25453A>T	ENSP00000378756.1:n.-36-25453A>T
ENST00000395348.7:c.-338A>T	ENSP00000378757.3:n.-338A>T
NM_194298.2:c.-338A>T	NP_919274.1:n.-338A>T
NM_001323977.1:c.-168+232A>T	NP_001310906.1:n.-168+232A>T
NM_001323978.1:c.-552A>T	NP_001310907.1:n.-552A>T
NM_001323979.1:c.-239A>T	NP_001310908.1:n.-239A>T
NM_001323980.1:c.-469A>T	NP_001310909.1:n.-469A>T
NM_001323981.1:c.-421A>T	NP_001310910.1:n.-421A>T
XM_017015883.1:c.-338A>T	XP_016871372.1:n.-338A>T
NM_001323978.2:c.-552A>T	NP_001310907.1:n.-552A>T
NM_001323979.2:c.-239A>T	NP_001310908.1:n.-239A>T
NM_001323980.2:c.-469A>T	NP_001310909.1:n.-469A>T
NM_001323981.2:c.-421A>T	NP_001310910.1:n.-421A>T
NM_194298.3:c.-338A>T MANE Select	NP_919274.1:n.-338A>T