Canonical Allele Identifier: CA1592684799

Gene: GALNT10

Linked Data

• dbSNP Id: rs1753084025

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227590del , CM000667.2:g.154227590del	GRCh38
NC_000005.9:g.153607150del , CM000667.1:g.153607150del	GRCh37
NC_000005.8:g.153587343del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36565del MANE Select	ENSP00000297107.6:n.159+36565del
ENST00000297107.10:c.159+36565del	ENSP00000297107.6:n.159+36565del
ENST00000377661.2:c.159+36565del	ENSP00000366889.2:n.159+36565del
ENST00000425427.6:c.159+36565del	ENSP00000415210.2:n.159+36565del
ENST00000520647.5:c.159+36565del	ENSP00000428573.1:n.159+36565del
ENST00000521781.5:n.150+9441del
NM_198321.3:c.159+36565del	NP_938080.1:n.159+36565del
NM_198321.4:c.159+36565del MANE Select	NP_938080.1:n.159+36565del