Canonical Allele Identifier: CA413658059
Gene: SLC16A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74525856G>T , CM000685.2:g.74525856G>T GRCh38
NC_000023.10:g.73745691G>T , CM000685.1:g.73745691G>T GRCh37
NC_000023.9:g.73662416G>T NCBI36
NG_011641.1:g.109607G>T
NG_011641.2:g.109607G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1133G>T MANE Select ENSP00000465734.1:p.Ser378Ile
ENST00000636771.1:c.1042G>T
ENST00000587091.5:c.1133G>T ENSP00000465734.1:p.Ser378Ile
ENST00000590447.1:c.573G>T
NM_006517.4:c.1133G>T NP_006508.2:p.Ser378Ile
XM_005262294.1:c.1133G>T XP_005262351.1:p.Ser378Ile
NM_006517.5:c.1133G>T MANE Select NP_006508.2:p.Ser378Ile