Canonical Allele Identifier: CA1592684902

Gene: GALNT10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227842_154227843delinsGT , CM000667.2:g.154227842_154227843delinsGT	GRCh38
NC_000005.9:g.153607402_153607403delinsGT , CM000667.1:g.153607402_153607403delinsGT	GRCh37
NC_000005.8:g.153587595_153587596delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36817_159+36818delinsGT MANE Select	ENSP00000297107.6:n.159+36817_159+36818delinsGT
ENST00000297107.10:c.159+36817_159+36818delinsGT	ENSP00000297107.6:n.159+36817_159+36818delinsGT
ENST00000377661.2:c.159+36817_159+36818delinsGT	ENSP00000366889.2:n.159+36817_159+36818delinsGT
ENST00000425427.6:c.159+36817_159+36818delinsGT	ENSP00000415210.2:n.159+36817_159+36818delinsGT
ENST00000520647.5:c.159+36817_159+36818delinsGT	ENSP00000428573.1:n.159+36817_159+36818delinsGT
ENST00000521781.5:n.150+9693_150+9694delinsGT
NM_198321.3:c.159+36817_159+36818delinsGT	NP_938080.1:n.159+36817_159+36818delinsGT
NM_198321.4:c.159+36817_159+36818delinsGT MANE Select	NP_938080.1:n.159+36817_159+36818delinsGT