Canonical Allele Identifier: CA2678053412
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859946_31860041del , CM000668.2:g.31859946_31860041del GRCh38
NC_000006.11:g.31827723_31827818del , CM000668.1:g.31827723_31827818del GRCh37
NC_000006.10:g.31935702_31935797del NCBI36
NG_008201.1:g.7893_7988del

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.1021+2_1022del
ENST00000677054.1:n.2266_2361del
ENST00000677512.1:n.1298+7_1299del
ENST00000678869.1:n.1609+2_1610del
ENST00000375631.4:c.1021+2_1022del
ENST00000480384.1:n.1226_1321del
ENST00000491768.5:c.*131+2_*132del
ENST00000495807.1:n.2329+2_2330del
NM_000434.3:c.1021+2_1022del
NM_000434.4:c.1021+2_1022del