Canonical Allele Identifier: CA1083142954
Gene: GALNT10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.154227786_154227787del , CM000667.2:g.154227786_154227787del GRCh38
NC_000005.9:g.153607346_153607347del , CM000667.1:g.153607346_153607347del GRCh37
NC_000005.8:g.153587539_153587540del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297107.11:c.159+36761_159+36762del MANE Select ENSP00000297107.6:n.159+36761_159+36762del
ENST00000297107.10:c.159+36761_159+36762del ENSP00000297107.6:n.159+36761_159+36762del
ENST00000377661.2:c.159+36761_159+36762del ENSP00000366889.2:n.159+36761_159+36762del
ENST00000425427.6:c.159+36761_159+36762del ENSP00000415210.2:n.159+36761_159+36762del
ENST00000520647.5:c.159+36761_159+36762del ENSP00000428573.1:n.159+36761_159+36762del
ENST00000521781.5:n.150+9637_150+9638del
NM_198321.3:c.159+36761_159+36762del NP_938080.1:n.159+36761_159+36762del
NM_198321.4:c.159+36761_159+36762del MANE Select NP_938080.1:n.159+36761_159+36762del