Canonical Allele Identifier: CA2710261062

Gene: GALNT10

Linked Data

• dbSNP Id: rs2113660087

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227386T>G , CM000667.2:g.154227386T>G	GRCh38
NC_000005.9:g.153606946T>G , CM000667.1:g.153606946T>G	GRCh37
NC_000005.8:g.153587139T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297107.11:c.159+36361T>G MANE Select	ENSP00000297107.6:n.159+36361T>G
ENST00000297107.10:c.159+36361T>G	ENSP00000297107.6:n.159+36361T>G
ENST00000377661.2:c.159+36361T>G	ENSP00000366889.2:n.159+36361T>G
ENST00000425427.6:c.159+36361T>G	ENSP00000415210.2:n.159+36361T>G
ENST00000520647.5:c.159+36361T>G	ENSP00000428573.1:n.159+36361T>G
ENST00000521781.5:n.150+9237T>G
NM_198321.3:c.159+36361T>G	NP_938080.1:n.159+36361T>G
NM_198321.4:c.159+36361T>G MANE Select	NP_938080.1:n.159+36361T>G