Canonical Allele Identifier: CA1592684749

Gene: GALNT10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227496_154227497delinsAT , CM000667.2:g.154227496_154227497delinsAT	GRCh38
NC_000005.9:g.153607056_153607057delinsAT , CM000667.1:g.153607056_153607057delinsAT	GRCh37
NC_000005.8:g.153587249_153587250delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36471_159+36472delinsAT MANE Select	ENSP00000297107.6:n.159+36471_159+36472delinsAT
ENST00000297107.10:c.159+36471_159+36472delinsAT	ENSP00000297107.6:n.159+36471_159+36472delinsAT
ENST00000377661.2:c.159+36471_159+36472delinsAT	ENSP00000366889.2:n.159+36471_159+36472delinsAT
ENST00000425427.6:c.159+36471_159+36472delinsAT	ENSP00000415210.2:n.159+36471_159+36472delinsAT
ENST00000520647.5:c.159+36471_159+36472delinsAT	ENSP00000428573.1:n.159+36471_159+36472delinsAT
ENST00000521781.5:n.150+9347_150+9348delinsAT
NM_198321.3:c.159+36471_159+36472delinsAT	NP_938080.1:n.159+36471_159+36472delinsAT
NM_198321.4:c.159+36471_159+36472delinsAT MANE Select	NP_938080.1:n.159+36471_159+36472delinsAT