Canonical Allele Identifier: CA130397554

Gene: GALNT10

Linked Data

• dbSNP Id: rs754103506
• gnomAD v2: 5-153607446-A-ATTTC
• gnomAD v3: 5-154227886-A-ATTTC
• gnomAD v4: 5-154227886-A-ATTTC
• MyVariant Identifiers: chr5:g.153607446_153607447insTTTC (hg19) ; chr5:g.154227886_154227887insTTTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227886_154227887insTTTC , CM000667.2:g.154227886_154227887insTTTC	GRCh38
NC_000005.9:g.153607446_153607447insTTTC , CM000667.1:g.153607446_153607447insTTTC	GRCh37
NC_000005.8:g.153587639_153587640insTTTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297107.11:c.159+36861_159+36862insTTTC MANE Select	ENSP00000297107.6:n.159+36861_159+36862insTTTC
ENST00000297107.10:c.159+36861_159+36862insTTTC	ENSP00000297107.6:n.159+36861_159+36862insTTTC
ENST00000377661.2:c.159+36861_159+36862insTTTC	ENSP00000366889.2:n.159+36861_159+36862insTTTC
ENST00000425427.6:c.159+36861_159+36862insTTTC	ENSP00000415210.2:n.159+36861_159+36862insTTTC
ENST00000520647.5:c.159+36861_159+36862insTTTC	ENSP00000428573.1:n.159+36861_159+36862insTTTC
ENST00000521781.5:n.150+9737_150+9738insTTTC
NM_198321.3:c.159+36861_159+36862insTTTC	NP_938080.1:n.159+36861_159+36862insTTTC
NM_198321.4:c.159+36861_159+36862insTTTC MANE Select	NP_938080.1:n.159+36861_159+36862insTTTC