Canonical Allele Identifier: CA1813618113
Gene: SLC30A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.117077252G= , CM000670.2:g.117077252G= GRCh38
NC_000008.10:g.118089491G= , CM000670.1:g.118089491G= GRCh37
NC_000008.9:g.118158672G= NCBI36
NG_016991.1:g.131980G=

Transcript Alleles

HGVS Amino-acid change
ENST00000427715.2:c.-226+37994G= ENSP00000407505.2:n.-226+37994G=
ENST00000521035.5:n.295-57980G=
ENST00000521243.5:c.-106-69567G= ENSP00000428545.1:n.-106-69567G=
ENST00000524274.5:c.-106-69567G= ENSP00000427760.1:n.-106-69567G=
NM_001172811.1:c.-106-69567G= NP_001166282.1:n.-106-69567G=
NM_001172813.1:c.-273-57980G= NP_001166284.1:n.-273-57980G=
NM_001172815.1:c.-226+37994G= NP_001166286.1:n.-226+37994G=
XM_011516881.1:c.-96-57980G= XP_011515183.1:n.-96-57980G=
NM_001172815.2:c.-226+37994G= NP_001166286.1:n.-226+37994G=
XM_024447083.1:c.-106-69567G= XP_024302851.1:n.-106-69567G=
NM_001172811.2:c.-106-69567G= NP_001166282.1:n.-106-69567G=
NM_001172813.2:c.-273-57980G= NP_001166284.1:n.-273-57980G=
NM_001172815.3:c.-226+37994G= NP_001166286.1:n.-226+37994G=