Canonical Allele Identifier: CA2678053426
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859972_31859978del , CM000668.2:g.31859972_31859978del GRCh38
NC_000006.11:g.31827749_31827755del , CM000668.1:g.31827749_31827755del GRCh37
NC_000006.10:g.31935728_31935734del NCBI36
NG_008201.1:g.7955_7961del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1022-33_1022-27del MANE Select ENSP00000364782.4:n.1022-33_1022-27del
ENST00000677054.1:n.2328_2334del
ENST00000677512.1:n.1299-33_1299-27del
ENST00000678869.1:n.1610-33_1610-27del
ENST00000375631.4:c.1022-33_1022-27del ENSP00000364782.4:n.1022-33_1022-27del
ENST00000480384.1:n.1288_1294del
ENST00000491768.5:c.*132-33_*132-27del ENSP00000433127.1:n.*132-33_*132-27del
ENST00000495807.1:n.2330-33_2330-27del
NM_000434.3:c.1022-33_1022-27del NP_000425.1:n.1022-33_1022-27del
NM_000434.4:c.1022-33_1022-27del MANE Select NP_000425.1:n.1022-33_1022-27del