Canonical Allele Identifier: CA130397507
Gene: GALNT10 HGNC NCBI

Linked Data

dbSNP Id: rs191133121
MyVariant Identifiers: chr5:g.153606963A>C (hg19) chr5:g.154227403A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227403A>C , CM000667.2:g.154227403A>C GRCh38
NC_000005.9:g.153606963A>C , CM000667.1:g.153606963A>C GRCh37
NC_000005.8:g.153587156A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297107.11:c.159+36378A>C MANE Select ENSP00000297107.6:n.159+36378A>C
ENST00000297107.10:c.159+36378A>C ENSP00000297107.6:n.159+36378A>C
ENST00000377661.2:c.159+36378A>C ENSP00000366889.2:n.159+36378A>C
ENST00000425427.6:c.159+36378A>C ENSP00000415210.2:n.159+36378A>C
ENST00000520647.5:c.159+36378A>C ENSP00000428573.1:n.159+36378A>C
ENST00000521781.5:n.150+9254A>C
NM_198321.3:c.159+36378A>C NP_938080.1:n.159+36378A>C
NM_198321.4:c.159+36378A>C MANE Select NP_938080.1:n.159+36378A>C
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