Canonical Allele Identifier: CA1592684703
Gene: GALNT10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227410A= , CM000667.2:g.154227410A= GRCh38
NC_000005.9:g.153606970A= , CM000667.1:g.153606970A= GRCh37
NC_000005.8:g.153587163A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297107.11:c.159+36385A= MANE Select ENSP00000297107.6:n.159+36385A=
ENST00000297107.10:c.159+36385A= ENSP00000297107.6:n.159+36385A=
ENST00000377661.2:c.159+36385A= ENSP00000366889.2:n.159+36385A=
ENST00000425427.6:c.159+36385A= ENSP00000415210.2:n.159+36385A=
ENST00000520647.5:c.159+36385A= ENSP00000428573.1:n.159+36385A=
ENST00000521781.5:n.150+9261A=
NM_198321.3:c.159+36385A= NP_938080.1:n.159+36385A=
NM_198321.4:c.159+36385A= MANE Select NP_938080.1:n.159+36385A=
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