Canonical Allele Identifier: CA2437509371
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74529143G= , CM000685.2:g.74529143G= GRCh38
NC_000023.10:g.73748978G= , CM000685.1:g.73748978G= GRCh37
NC_000023.9:g.73665703G= NCBI36
NG_011641.1:g.112894G=
NG_011641.2:g.112894G=

Transcript Alleles

HGVS Amino-acid change
ENST00000587091.6:c.1171-70G= MANE Select ENSP00000465734.1:n.1171-70G=
ENST00000636771.1:c.1080-70G=
ENST00000587091.5:c.1171-70G= ENSP00000465734.1:n.1171-70G=
ENST00000590447.1:c.611-2190G=
NM_006517.4:c.1171-70G= NP_006508.2:n.1171-70G=
XM_005262294.1:c.1171-2190G= XP_005262351.1:n.1171-2190G=
NM_006517.5:c.1171-70G= MANE Select NP_006508.2:n.1171-70G=