Canonical Allele Identifier: CA1592684870

Gene: GALNT10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227757_154227760delinsTCCC , CM000667.2:g.154227757_154227760delinsTCCC	GRCh38
NC_000005.9:g.153607317_153607320delinsTCCC , CM000667.1:g.153607317_153607320delinsTCCC	GRCh37
NC_000005.8:g.153587510_153587513delinsTCCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36732_159+36735delinsTCCC MANE Select	ENSP00000297107.6:n.159+36732_159+36735delinsTCCC
ENST00000297107.10:c.159+36732_159+36735delinsTCCC	ENSP00000297107.6:n.159+36732_159+36735delinsTCCC
ENST00000377661.2:c.159+36732_159+36735delinsTCCC	ENSP00000366889.2:n.159+36732_159+36735delinsTCCC
ENST00000425427.6:c.159+36732_159+36735delinsTCCC	ENSP00000415210.2:n.159+36732_159+36735delinsTCCC
ENST00000520647.5:c.159+36732_159+36735delinsTCCC	ENSP00000428573.1:n.159+36732_159+36735delinsTCCC
ENST00000521781.5:n.150+9608_150+9611delinsTCCC
NM_198321.3:c.159+36732_159+36735delinsTCCC	NP_938080.1:n.159+36732_159+36735delinsTCCC
NM_198321.4:c.159+36732_159+36735delinsTCCC MANE Select	NP_938080.1:n.159+36732_159+36735delinsTCCC