Canonical Allele Identifier: CA208159534

Gene: SLC16A9

Linked Data

• dbSNP Id: rs1171617
• gnomAD v2: 10-61467182-G-T
• gnomAD v3: 10-59707424-G-T
• gnomAD v4: 10-59707424-G-T
• MyVariant Identifiers: chr10:g.61467182G>T (hg19) ; chr10:g.59707424G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.59707424G>T , CM000672.2:g.59707424G>T	GRCh38
NC_000010.10:g.61467182G>T , CM000672.1:g.61467182G>T	GRCh37
NC_000010.9:g.61137188G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395348.8:c.-37+2055C>A MANE Select	ENSP00000378757.3:n.-37+2055C>A
ENST00000395347.1:c.-36-23097C>A	ENSP00000378756.1:n.-36-23097C>A
ENST00000395348.7:c.-37+2055C>A	ENSP00000378757.3:n.-37+2055C>A
ENST00000490066.1:n.222+1182C>A
NM_194298.2:c.-37+2055C>A	NP_919274.1:n.-37+2055C>A
NM_001323977.1:c.-168+2588C>A	NP_001310906.1:n.-168+2588C>A
NM_001323978.1:c.-250-236C>A	NP_001310907.1:n.-250-236C>A
NM_001323979.1:c.-168+2285C>A	NP_001310908.1:n.-168+2285C>A
NM_001323980.1:c.-168+2055C>A	NP_001310909.1:n.-168+2055C>A
NM_001323981.1:c.-119-236C>A	NP_001310910.1:n.-119-236C>A
XM_017015883.1:c.-37+2055C>A	XP_016871372.1:n.-37+2055C>A
XM_017015884.2:c.-182+2055C>A	XP_016871373.1:n.-182+2055C>A
NM_001323978.2:c.-250-236C>A	NP_001310907.1:n.-250-236C>A
NM_001323979.2:c.-168+2285C>A	NP_001310908.1:n.-168+2285C>A
NM_001323980.2:c.-168+2055C>A	NP_001310909.1:n.-168+2055C>A
NM_001323981.2:c.-119-236C>A	NP_001310910.1:n.-119-236C>A
NM_194298.3:c.-37+2055C>A MANE Select	NP_919274.1:n.-37+2055C>A