Canonical Allele Identifier: CA1813618118
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117077257T= , CM000670.2:g.117077257T= GRCh38
NC_000008.10:g.118089496T= , CM000670.1:g.118089496T= GRCh37
NC_000008.9:g.118158677T= NCBI36
NG_016991.1:g.131985T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000427715.2:c.-226+37999T= ENSP00000407505.2:n.-226+37999T=
ENST00000521035.5:n.295-57975T=
ENST00000521243.5:c.-106-69562T= ENSP00000428545.1:n.-106-69562T=
ENST00000524274.5:c.-106-69562T= ENSP00000427760.1:n.-106-69562T=
NM_001172811.1:c.-106-69562T= NP_001166282.1:n.-106-69562T=
NM_001172813.1:c.-273-57975T= NP_001166284.1:n.-273-57975T=
NM_001172815.1:c.-226+37999T= NP_001166286.1:n.-226+37999T=
XM_011516881.1:c.-96-57975T= XP_011515183.1:n.-96-57975T=
NM_001172815.2:c.-226+37999T= NP_001166286.1:n.-226+37999T=
XM_024447083.1:c.-106-69562T= XP_024302851.1:n.-106-69562T=
NM_001172811.2:c.-106-69562T= NP_001166282.1:n.-106-69562T=
NM_001172813.2:c.-273-57975T= NP_001166284.1:n.-273-57975T=
NM_001172815.3:c.-226+37999T= NP_001166286.1:n.-226+37999T=