Canonical Allele Identifier: CA130397531
Gene: GALNT10 HGNC NCBI

Linked Data

dbSNP Id: rs939127972
MyVariant Identifiers: chr5:g.154227602G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227602G>A , CM000667.2:g.154227602G>A GRCh38
NC_000005.9:g.153607162G>A , CM000667.1:g.153607162G>A GRCh37
NC_000005.8:g.153587355G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297107.11:c.159+36577G>A MANE Select ENSP00000297107.6:n.159+36577G>A
ENST00000297107.10:c.159+36577G>A ENSP00000297107.6:n.159+36577G>A
ENST00000377661.2:c.159+36577G>A ENSP00000366889.2:n.159+36577G>A
ENST00000425427.6:c.159+36577G>A ENSP00000415210.2:n.159+36577G>A
ENST00000520647.5:c.159+36577G>A ENSP00000428573.1:n.159+36577G>A
ENST00000521781.5:n.150+9453G>A
NM_198321.3:c.159+36577G>A NP_938080.1:n.159+36577G>A
NM_198321.4:c.159+36577G>A MANE Select NP_938080.1:n.159+36577G>A
Search 100 bp 5'
Search 100 bp 3'