Canonical Allele Identifier: CA563862307

Gene: GALNT10

Linked Data

• dbSNP Id: rs1321224858
• gnomAD v2: 5-153606923-ATATCT-A
• gnomAD v3: 5-154227363-ATATCT-A
• gnomAD v4: 5-154227363-ATATCT-A
• MyVariant Identifiers: chr5:g.153606924_153606928del (hg19) ; chr5:g.154227364_154227368del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227366_154227370del , CM000667.2:g.154227366_154227370del	GRCh38
NC_000005.9:g.153606926_153606930del , CM000667.1:g.153606926_153606930del	GRCh37
NC_000005.8:g.153587119_153587123del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36341_159+36345del MANE Select	ENSP00000297107.6:n.159+36341_159+36345del
ENST00000297107.10:c.159+36341_159+36345del	ENSP00000297107.6:n.159+36341_159+36345del
ENST00000377661.2:c.159+36341_159+36345del	ENSP00000366889.2:n.159+36341_159+36345del
ENST00000425427.6:c.159+36341_159+36345del	ENSP00000415210.2:n.159+36341_159+36345del
ENST00000520647.5:c.159+36341_159+36345del	ENSP00000428573.1:n.159+36341_159+36345del
ENST00000521781.5:n.150+9217_150+9221del
NM_198321.3:c.159+36341_159+36345del	NP_938080.1:n.159+36341_159+36345del
NM_198321.4:c.159+36341_159+36345del MANE Select	NP_938080.1:n.159+36341_159+36345del