Canonical Allele Identifier: CA1619341587
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859645_31859649delinsGCAGA , CM000668.2:g.31859645_31859649delinsGCAGA GRCh38
NC_000006.11:g.31827422_31827426delinsGCAGA , CM000668.1:g.31827422_31827426delinsGCAGA GRCh37
NC_000006.10:g.31935401_31935405delinsGCAGA NCBI36
NG_008201.1:g.8284_8288delinsTCTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.*70_*74delinsTCTGC MANE Select ENSP00000364782.4:n.*70_*74delinsTCTGC
ENST00000677054.1:n.2657_2661delinsTCTGC
ENST00000677512.1:n.1595_1599delinsTCTGC
ENST00000678869.1:n.1906_1910delinsTCTGC
ENST00000375631.4:c.*70_*74delinsTCTGC ENSP00000364782.4:n.*70_*74delinsTCTGC
ENST00000480384.1:n.1617_1621delinsTCTGC
ENST00000491768.5:c.*428_*432delinsTCTGC ENSP00000433127.1:n.*428_*432delinsTCTGC
ENST00000495807.1:n.2626_2630delinsTCTGC
NM_000434.3:c.*70_*74delinsTCTGC NP_000425.1:n.*70_*74delinsTCTGC
NM_000434.4:c.*70_*74delinsTCTGC MANE Select NP_000425.1:n.*70_*74delinsTCTGC
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