Canonical Allele Identifier: CA2710261153

Gene: GALNT10

Linked Data

• dbSNP Id: rs2113660404

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227888_154227889insAG , CM000667.2:g.154227888_154227889insAG	GRCh38
NC_000005.9:g.153607448_153607449insAG , CM000667.1:g.153607448_153607449insAG	GRCh37
NC_000005.8:g.153587641_153587642insAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36863_159+36864insAG MANE Select	ENSP00000297107.6:n.159+36863_159+36864insAG
ENST00000297107.10:c.159+36863_159+36864insAG	ENSP00000297107.6:n.159+36863_159+36864insAG
ENST00000377661.2:c.159+36863_159+36864insAG	ENSP00000366889.2:n.159+36863_159+36864insAG
ENST00000425427.6:c.159+36863_159+36864insAG	ENSP00000415210.2:n.159+36863_159+36864insAG
ENST00000520647.5:c.159+36863_159+36864insAG	ENSP00000428573.1:n.159+36863_159+36864insAG
ENST00000521781.5:n.150+9739_150+9740insAG
NM_198321.3:c.159+36863_159+36864insAG	NP_938080.1:n.159+36863_159+36864insAG
NM_198321.4:c.159+36863_159+36864insAG MANE Select	NP_938080.1:n.159+36863_159+36864insAG