Canonical Allele Identifier: CA2013297305
Gene: GALNT8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4754173G= , CM000674.2:g.4754173G= GRCh38
NC_000012.11:g.4863339G= , CM000674.1:g.4863339G= GRCh37
NC_000012.10:g.4733600G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252318.7:c.1174-6785G= MANE Select ENSP00000252318.2:n.1174-6785G=
ENST00000648836.1:c.964-6785G= ENSP00000497305.1:n.964-6785G=
ENST00000648865.1:n.26-6785G=
ENST00000252318.6:c.1174-6785G= ENSP00000252318.2:n.1174-6785G=
NM_017417.1:c.1174-6785G= NP_059113.1:n.1174-6785G=
NM_017417.2:c.1174-6785G= MANE Select NP_059113.1:n.1174-6785G=
Search 100 bp 5'
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