Canonical Allele Identifier: CA130397511

Gene: GALNT10

Linked Data

• dbSNP Id: rs964109034
• gnomAD v2: 5-153606993-T-C
• gnomAD v3: 5-154227433-T-C
• gnomAD v4: 5-154227433-T-C
• MyVariant Identifiers: chr5:g.153606993T>C (hg19) ; chr5:g.154227433T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.154227433T>C , CM000667.2:g.154227433T>C	GRCh38
NC_000005.9:g.153606993T>C , CM000667.1:g.153606993T>C	GRCh37
NC_000005.8:g.153587186T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297107.11:c.159+36408T>C MANE Select	ENSP00000297107.6:n.159+36408T>C
ENST00000297107.10:c.159+36408T>C	ENSP00000297107.6:n.159+36408T>C
ENST00000377661.2:c.159+36408T>C	ENSP00000366889.2:n.159+36408T>C
ENST00000425427.6:c.159+36408T>C	ENSP00000415210.2:n.159+36408T>C
ENST00000520647.5:c.159+36408T>C	ENSP00000428573.1:n.159+36408T>C
ENST00000521781.5:n.150+9284T>C
NM_198321.3:c.159+36408T>C	NP_938080.1:n.159+36408T>C
NM_198321.4:c.159+36408T>C MANE Select	NP_938080.1:n.159+36408T>C