Canonical Allele Identifier: CA2710087942
Gene: GALNT10 HGNC NCBI

Linked Data

dbSNP Id: rs1561634756

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227387A>T , CM000667.2:g.154227387A>T GRCh38
NC_000005.9:g.153606947A>T , CM000667.1:g.153606947A>T GRCh37
NC_000005.8:g.153587140A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000297107.11:c.159+36362A>T MANE Select ENSP00000297107.6:n.159+36362A>T
ENST00000297107.10:c.159+36362A>T ENSP00000297107.6:n.159+36362A>T
ENST00000377661.2:c.159+36362A>T ENSP00000366889.2:n.159+36362A>T
ENST00000425427.6:c.159+36362A>T ENSP00000415210.2:n.159+36362A>T
ENST00000520647.5:c.159+36362A>T ENSP00000428573.1:n.159+36362A>T
ENST00000521781.5:n.150+9238A>T
NM_198321.3:c.159+36362A>T NP_938080.1:n.159+36362A>T
NM_198321.4:c.159+36362A>T MANE Select NP_938080.1:n.159+36362A>T