Canonical Allele Identifier: CA1619341711
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859951G= , CM000668.2:g.31859951G= GRCh38
NC_000006.11:g.31827728G= , CM000668.1:g.31827728G= GRCh37
NC_000006.10:g.31935707G= NCBI36
NG_008201.1:g.7982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1022-6C= MANE Select ENSP00000364782.4:n.1022-6C=
ENST00000677054.1:n.2355C=
ENST00000677512.1:n.1299-6C=
ENST00000678869.1:n.1610-6C=
ENST00000375631.4:c.1022-6C= ENSP00000364782.4:n.1022-6C=
ENST00000480384.1:n.1315C=
ENST00000491768.5:c.*132-6C= ENSP00000433127.1:n.*132-6C=
ENST00000495807.1:n.2330-6C=
NM_000434.3:c.1022-6C= NP_000425.1:n.1022-6C=
NM_000434.4:c.1022-6C= MANE Select NP_000425.1:n.1022-6C=
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