Canonical Allele Identifier: CA666987882

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1326208652
• gnomAD v3: 10-59709336-C-T
• gnomAD v4: 10-59709336-C-T
• MyVariant Identifiers: chr10:g.61469094C>T (hg19) ; chr10:g.59709336C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709336C>T , CM000672.2:g.59709336C>T	GRCh38
NC_000010.10:g.61469094C>T , CM000672.1:g.61469094C>T	GRCh37
NC_000010.9:g.61139100C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+143G>A MANE Select	ENSP00000378757.3:n.-37+143G>A
ENST00000395347.1:c.-36-25009G>A	ENSP00000378756.1:n.-36-25009G>A
ENST00000395348.7:c.-37+143G>A	ENSP00000378757.3:n.-37+143G>A
ENST00000490066.1:n.44+143G>A
NM_194298.2:c.-37+143G>A	NP_919274.1:n.-37+143G>A
NM_001323977.1:c.-168+676G>A	NP_001310906.1:n.-168+676G>A
NM_001323978.1:c.-251+143G>A	NP_001310907.1:n.-251+143G>A
NM_001323979.1:c.-168+373G>A	NP_001310908.1:n.-168+373G>A
NM_001323980.1:c.-168+143G>A	NP_001310909.1:n.-168+143G>A
NM_001323981.1:c.-120+143G>A	NP_001310910.1:n.-120+143G>A
XM_017015883.1:c.-37+143G>A	XP_016871372.1:n.-37+143G>A
XM_017015884.2:c.-182+143G>A	XP_016871373.1:n.-182+143G>A
NM_001323978.2:c.-251+143G>A	NP_001310907.1:n.-251+143G>A
NM_001323979.2:c.-168+373G>A	NP_001310908.1:n.-168+373G>A
NM_001323980.2:c.-168+143G>A	NP_001310909.1:n.-168+143G>A
NM_001323981.2:c.-120+143G>A	NP_001310910.1:n.-120+143G>A
NM_194298.3:c.-37+143G>A MANE Select	NP_919274.1:n.-37+143G>A