Canonical Allele Identifier: CA805902913

Gene: GALNT10

Linked Data

• dbSNP Id: rs1402164094
• MyVariant Identifiers: chr5:g.153607317_153607318insC (hg19) ; chr5:g.154227757_154227758insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227760dup , CM000667.2:g.154227760dup	GRCh38
NC_000005.9:g.153607320dup , CM000667.1:g.153607320dup	GRCh37
NC_000005.8:g.153587513dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36735dup MANE Select	ENSP00000297107.6:n.159+36735dup
ENST00000297107.10:c.159+36735dup	ENSP00000297107.6:n.159+36735dup
ENST00000377661.2:c.159+36735dup	ENSP00000366889.2:n.159+36735dup
ENST00000425427.6:c.159+36735dup	ENSP00000415210.2:n.159+36735dup
ENST00000520647.5:c.159+36735dup	ENSP00000428573.1:n.159+36735dup
ENST00000521781.5:n.150+9611dup
NM_198321.3:c.159+36735dup	NP_938080.1:n.159+36735dup
NM_198321.4:c.159+36735dup MANE Select	NP_938080.1:n.159+36735dup