Canonical Allele Identifier: CA563862375

Gene: GALNT10

Linked Data

• gnomAD v2: 5-153607322-TATG-T
• gnomAD v3: 5-154227762-TATG-T
• gnomAD v4: 5-154227762-TATG-T
• MyVariant Identifiers: chr5:g.153607323_153607325del (hg19) ; chr5:g.154227763_154227765del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227763_154227765del , CM000667.2:g.154227763_154227765del	GRCh38
NC_000005.9:g.153607323_153607325del , CM000667.1:g.153607323_153607325del	GRCh37
NC_000005.8:g.153587516_153587518del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36738_159+36740del MANE Select	ENSP00000297107.6:n.159+36738_159+36740del
ENST00000297107.10:c.159+36738_159+36740del	ENSP00000297107.6:n.159+36738_159+36740del
ENST00000377661.2:c.159+36738_159+36740del	ENSP00000366889.2:n.159+36738_159+36740del
ENST00000425427.6:c.159+36738_159+36740del	ENSP00000415210.2:n.159+36738_159+36740del
ENST00000520647.5:c.159+36738_159+36740del	ENSP00000428573.1:n.159+36738_159+36740del
ENST00000521781.5:n.150+9614_150+9616del
NM_198321.3:c.159+36738_159+36740del	NP_938080.1:n.159+36738_159+36740del
NM_198321.4:c.159+36738_159+36740del MANE Select	NP_938080.1:n.159+36738_159+36740del