Canonical Allele Identifier: CA1083142945
Gene: GALNT10 HGNC NCBI

Linked Data

gnomAD v3: 5-154227784-A-T
gnomAD v4: 5-154227784-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227784A>T , CM000667.2:g.154227784A>T GRCh38
NC_000005.9:g.153607344A>T , CM000667.1:g.153607344A>T GRCh37
NC_000005.8:g.153587537A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297107.11:c.159+36759A>T MANE Select ENSP00000297107.6:n.159+36759A>T
ENST00000297107.10:c.159+36759A>T ENSP00000297107.6:n.159+36759A>T
ENST00000377661.2:c.159+36759A>T ENSP00000366889.2:n.159+36759A>T
ENST00000425427.6:c.159+36759A>T ENSP00000415210.2:n.159+36759A>T
ENST00000520647.5:c.159+36759A>T ENSP00000428573.1:n.159+36759A>T
ENST00000521781.5:n.150+9635A>T
NM_198321.3:c.159+36759A>T NP_938080.1:n.159+36759A>T
NM_198321.4:c.159+36759A>T MANE Select NP_938080.1:n.159+36759A>T
Search 100 bp 5'
Search 100 bp 3'