Canonical Allele Identifier: CA5509949
Gene: SLC16A9 HGNC NCBI

Linked Data

dbSNP Id: rs2242206

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.59654253G>T , CM000672.2:g.59654253G>T GRCh38
NC_000010.10:g.61414011G>T , CM000672.1:g.61414011G>T GRCh37
NC_000010.9:g.61084017G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395348.8:c.773C>A MANE Select ENSP00000378757.3:p.Thr258Lys
ENST00000395347.1:c.773C>A ENSP00000378756.1:p.Thr258Lys
ENST00000395348.7:c.773C>A ENSP00000378757.3:p.Thr258Lys
NM_194298.2:c.773C>A NP_919274.1:p.Thr258Lys
XM_011539488.1:c.773C>A XP_011537790.1:p.Thr258Lys
NM_001323977.1:c.512C>A NP_001310906.1:p.Thr171Lys
NM_001323978.1:c.512C>A NP_001310907.1:p.Thr171Lys
NM_001323979.1:c.512C>A NP_001310908.1:p.Thr171Lys
NM_001323980.1:c.512C>A NP_001310909.1:p.Thr171Lys
NM_001323981.1:c.773C>A NP_001310910.1:p.Thr258Lys
XM_017015883.1:c.773C>A XP_016871372.1:p.Thr258Lys
XM_017015884.2:c.773C>A XP_016871373.1:p.Thr258Lys
XM_024447878.1:c.773C>A XP_024303646.1:p.Thr258Lys
NM_001323978.2:c.512C>A NP_001310907.1:p.Thr171Lys
NM_001323979.2:c.512C>A NP_001310908.1:p.Thr171Lys
NM_001323980.2:c.512C>A NP_001310909.1:p.Thr171Lys
NM_001323981.2:c.773C>A NP_001310910.1:p.Thr258Lys
NM_194298.3:c.773C>A MANE Select NP_919274.1:p.Thr258Lys