Canonical Allele Identifier: CA2013297304
Gene: GALNT8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4754169G= , CM000674.2:g.4754169G= GRCh38
NC_000012.11:g.4863335G= , CM000674.1:g.4863335G= GRCh37
NC_000012.10:g.4733596G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252318.7:c.1174-6789G= MANE Select ENSP00000252318.2:n.1174-6789G=
ENST00000648836.1:c.964-6789G= ENSP00000497305.1:n.964-6789G=
ENST00000648865.1:n.26-6789G=
ENST00000252318.6:c.1174-6789G= ENSP00000252318.2:n.1174-6789G=
NM_017417.1:c.1174-6789G= NP_059113.1:n.1174-6789G=
NM_017417.2:c.1174-6789G= MANE Select NP_059113.1:n.1174-6789G=