Canonical Allele Identifier: CA1619341720
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859968G= , CM000668.2:g.31859968G= GRCh38
NC_000006.11:g.31827745G= , CM000668.1:g.31827745G= GRCh37
NC_000006.10:g.31935724G= NCBI36
NG_008201.1:g.7965C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.1022-23C= MANE Select ENSP00000364782.4:n.1022-23C=
ENST00000677054.1:n.2338C=
ENST00000677512.1:n.1299-23C=
ENST00000678869.1:n.1610-23C=
ENST00000375631.4:c.1022-23C= ENSP00000364782.4:n.1022-23C=
ENST00000480384.1:n.1298C=
ENST00000491768.5:c.*132-23C= ENSP00000433127.1:n.*132-23C=
ENST00000495807.1:n.2330-23C=
NM_000434.3:c.1022-23C= NP_000425.1:n.1022-23C=
NM_000434.4:c.1022-23C= MANE Select NP_000425.1:n.1022-23C=
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