Canonical Allele Identifier: CA1592684688

Gene: GALNT10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227370_154227383delinsAACGTGGTTTTAAT , CM000667.2:g.154227370_154227383delinsAACGTGGTTTTAAT	GRCh38
NC_000005.9:g.153606930_153606943delinsAACGTGGTTTTAAT , CM000667.1:g.153606930_153606943delinsAACGTGGTTTTAAT	GRCh37
NC_000005.8:g.153587123_153587136delinsAACGTGGTTTTAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297107.11:c.159+36345_159+36358delinsAACGTGGTTTTAAT MANE Select	ENSP00000297107.6:n.159+36345_159+36358delinsAACGTGGTTTTAAT
ENST00000297107.10:c.159+36345_159+36358delinsAACGTGGTTTTAAT	ENSP00000297107.6:n.159+36345_159+36358delinsAACGTGGTTTTAAT
ENST00000377661.2:c.159+36345_159+36358delinsAACGTGGTTTTAAT	ENSP00000366889.2:n.159+36345_159+36358delinsAACGTGGTTTTAAT
ENST00000425427.6:c.159+36345_159+36358delinsAACGTGGTTTTAAT	ENSP00000415210.2:n.159+36345_159+36358delinsAACGTGGTTTTAAT
ENST00000520647.5:c.159+36345_159+36358delinsAACGTGGTTTTAAT	ENSP00000428573.1:n.159+36345_159+36358delinsAACGTGGTTTTAAT
ENST00000521781.5:n.150+9221_150+9234delinsAACGTGGTTTTAAT
NM_198321.3:c.159+36345_159+36358delinsAACGTGGTTTTAAT	NP_938080.1:n.159+36345_159+36358delinsAACGTGGTTTTAAT
NM_198321.4:c.159+36345_159+36358delinsAACGTGGTTTTAAT MANE Select	NP_938080.1:n.159+36345_159+36358delinsAACGTGGTTTTAAT