Canonical Allele Identifier: CA928947977

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1300266991
• gnomAD v3: 10-59709351-C-T
• gnomAD v4: 10-59709351-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59709351C>T , CM000672.2:g.59709351C>T	GRCh38
NC_000010.10:g.61469109C>T , CM000672.1:g.61469109C>T	GRCh37
NC_000010.9:g.61139115C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395348.8:c.-37+128G>A MANE Select	ENSP00000378757.3:n.-37+128G>A
ENST00000395347.1:c.-36-25024G>A	ENSP00000378756.1:n.-36-25024G>A
ENST00000395348.7:c.-37+128G>A	ENSP00000378757.3:n.-37+128G>A
ENST00000490066.1:n.44+128G>A
NM_194298.2:c.-37+128G>A	NP_919274.1:n.-37+128G>A
NM_001323977.1:c.-168+661G>A	NP_001310906.1:n.-168+661G>A
NM_001323978.1:c.-251+128G>A	NP_001310907.1:n.-251+128G>A
NM_001323979.1:c.-168+358G>A	NP_001310908.1:n.-168+358G>A
NM_001323980.1:c.-168+128G>A	NP_001310909.1:n.-168+128G>A
NM_001323981.1:c.-120+128G>A	NP_001310910.1:n.-120+128G>A
XM_017015883.1:c.-37+128G>A	XP_016871372.1:n.-37+128G>A
XM_017015884.2:c.-182+128G>A	XP_016871373.1:n.-182+128G>A
NM_001323978.2:c.-251+128G>A	NP_001310907.1:n.-251+128G>A
NM_001323979.2:c.-168+358G>A	NP_001310908.1:n.-168+358G>A
NM_001323980.2:c.-168+128G>A	NP_001310909.1:n.-168+128G>A
NM_001323981.2:c.-120+128G>A	NP_001310910.1:n.-120+128G>A
NM_194298.3:c.-37+128G>A MANE Select	NP_919274.1:n.-37+128G>A