Canonical Allele Identifier: CA377064406
Gene: SLC16A9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.59654263T>A , CM000672.2:g.59654263T>A GRCh38
NC_000010.10:g.61414021T>A , CM000672.1:g.61414021T>A GRCh37
NC_000010.9:g.61084027T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395348.8:c.763A>T MANE Select ENSP00000378757.3:p.Lys255Ter
ENST00000395347.1:c.763A>T ENSP00000378756.1:p.Lys255Ter
ENST00000395348.7:c.763A>T ENSP00000378757.3:p.Lys255Ter
NM_194298.2:c.763A>T NP_919274.1:p.Lys255Ter
XM_011539488.1:c.763A>T XP_011537790.1:p.Lys255Ter
NM_001323977.1:c.502A>T NP_001310906.1:p.Lys168Ter
NM_001323978.1:c.502A>T NP_001310907.1:p.Lys168Ter
NM_001323979.1:c.502A>T NP_001310908.1:p.Lys168Ter
NM_001323980.1:c.502A>T NP_001310909.1:p.Lys168Ter
NM_001323981.1:c.763A>T NP_001310910.1:p.Lys255Ter
XM_017015883.1:c.763A>T XP_016871372.1:p.Lys255Ter
XM_017015884.2:c.763A>T XP_016871373.1:p.Lys255Ter
XM_024447878.1:c.763A>T XP_024303646.1:p.Lys255Ter
NM_001323978.2:c.502A>T NP_001310907.1:p.Lys168Ter
NM_001323979.2:c.502A>T NP_001310908.1:p.Lys168Ter
NM_001323980.2:c.502A>T NP_001310909.1:p.Lys168Ter
NM_001323981.2:c.763A>T NP_001310910.1:p.Lys255Ter
NM_194298.3:c.763A>T MANE Select NP_919274.1:p.Lys255Ter