Canonical Allele Identifier: CA413658500
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529369C>T , CM000685.2:g.74529369C>T GRCh38
NC_000023.10:g.73749204C>T , CM000685.1:g.73749204C>T GRCh37
NC_000023.9:g.73665929C>T NCBI36
NG_011641.1:g.113120C>T
NG_011641.2:g.113120C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1327C>T MANE Select ENSP00000465734.1:p.Gln443Ter
ENST00000636771.1:c.1236C>T
ENST00000587091.5:c.1327C>T ENSP00000465734.1:p.Gln443Ter
ENST00000590447.1:c.611-1964C>T
NM_006517.4:c.1327C>T NP_006508.2:p.Gln443Ter
XM_005262294.1:c.1171-1964C>T XP_005262351.1:n.1171-1964C>T
NM_006517.5:c.1327C>T MANE Select NP_006508.2:p.Gln443Ter