Canonical Allele Identifier: CA2678053908
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861181_31861191del , CM000668.2:g.31861181_31861191del GRCh38
NC_000006.11:g.31828958_31828968del , CM000668.1:g.31828958_31828968del GRCh37
NC_000006.10:g.31936937_31936947del NCBI36
NG_008201.1:g.6744_6754del

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.614_615+9del
ENST00000677054.1:n.1291_1301del
ENST00000677512.1:n.722_723+9del
ENST00000678869.1:n.722_732del
ENST00000375631.4:c.614_615+9del
ENST00000480384.1:n.643_644+9del
ENST00000491768.5:c.614_615+9del
ENST00000495807.1:n.1182_1192del
NM_000434.3:c.614_615+9del
NM_000434.4:c.614_615+9del