Canonical Allele Identifier: CA130397501

Gene: GALNT10

Linked Data

• dbSNP Id: rs890374231
• gnomAD v2: 5-153606930-AACGTGGTTTTAAT-A
• gnomAD v3: 5-154227370-AACGTGGTTTTAAT-A
• gnomAD v4: 5-154227370-AACGTGGTTTTAAT-A
• MyVariant Identifiers: chr5:g.153606931_153606943del (hg19) ; chr5:g.154227371_154227383del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227371_154227383del , CM000667.2:g.154227371_154227383del	GRCh38
NC_000005.9:g.153606931_153606943del , CM000667.1:g.153606931_153606943del	GRCh37
NC_000005.8:g.153587124_153587136del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297107.11:c.159+36346_159+36358del MANE Select	ENSP00000297107.6:n.159+36346_159+36358del
ENST00000297107.10:c.159+36346_159+36358del	ENSP00000297107.6:n.159+36346_159+36358del
ENST00000377661.2:c.159+36346_159+36358del	ENSP00000366889.2:n.159+36346_159+36358del
ENST00000425427.6:c.159+36346_159+36358del	ENSP00000415210.2:n.159+36346_159+36358del
ENST00000520647.5:c.159+36346_159+36358del	ENSP00000428573.1:n.159+36346_159+36358del
ENST00000521781.5:n.150+9222_150+9234del
NM_198321.3:c.159+36346_159+36358del	NP_938080.1:n.159+36346_159+36358del
NM_198321.4:c.159+36346_159+36358del MANE Select	NP_938080.1:n.159+36346_159+36358del