Canonical Allele Identifier: CA2437509381
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529181C= , CM000685.2:g.74529181C= GRCh38
NC_000023.10:g.73749016C= , CM000685.1:g.73749016C= GRCh37
NC_000023.9:g.73665741C= NCBI36
NG_011641.1:g.112932C=
NG_011641.2:g.112932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.1171-32C= MANE Select ENSP00000465734.1:n.1171-32C=
ENST00000636771.1:c.1080-32C=
ENST00000587091.5:c.1171-32C= ENSP00000465734.1:n.1171-32C=
ENST00000590447.1:c.611-2152C=
NM_006517.4:c.1171-32C= NP_006508.2:n.1171-32C=
XM_005262294.1:c.1171-2152C= XP_005262351.1:n.1171-2152C=
NM_006517.5:c.1171-32C= MANE Select NP_006508.2:n.1171-32C=