Canonical Allele Identifier: CA2710261106
Gene: GALNT10 HGNC NCBI

Linked Data

dbSNP Id: rs2113660106
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227418C>A , CM000667.2:g.154227418C>A GRCh38
NC_000005.9:g.153606978C>A , CM000667.1:g.153606978C>A GRCh37
NC_000005.8:g.153587171C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297107.11:c.159+36393C>A MANE Select ENSP00000297107.6:n.159+36393C>A
ENST00000297107.10:c.159+36393C>A ENSP00000297107.6:n.159+36393C>A
ENST00000377661.2:c.159+36393C>A ENSP00000366889.2:n.159+36393C>A
ENST00000425427.6:c.159+36393C>A ENSP00000415210.2:n.159+36393C>A
ENST00000520647.5:c.159+36393C>A ENSP00000428573.1:n.159+36393C>A
ENST00000521781.5:n.150+9269C>A
NM_198321.3:c.159+36393C>A NP_938080.1:n.159+36393C>A
NM_198321.4:c.159+36393C>A MANE Select NP_938080.1:n.159+36393C>A
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