Canonical Allele Identifier: CA13244767

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1171614
• gnomAD v2: 10-61469538-T-C
• gnomAD v3: 10-59709780-T-C
• gnomAD v4: 10-59709780-T-C
• MyVariant Identifiers: chr10:g.61469538T>C (hg19) ; chr10:g.59709780T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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