Canonical Allele Identifier: CA1619342365
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861563C= , CM000668.2:g.31861563C= GRCh38
NC_000006.11:g.31829340C= , CM000668.1:g.31829340C= GRCh37
NC_000006.10:g.31937319C= NCBI36
NG_008201.1:g.6370G=
NG_023058.1:g.22484G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-113G= MANE Select ENSP00000364782.4:n.353-113G=
ENST00000677054.1:n.917G=
ENST00000677512.1:n.461-113G=
ENST00000678869.1:n.461-113G=
ENST00000375631.4:c.353-113G= ENSP00000364782.4:n.353-113G=
ENST00000480384.1:n.382-113G=
ENST00000491768.5:c.353-113G= ENSP00000433127.1:n.353-113G=
ENST00000495807.1:n.808G=
NM_000434.3:c.353-113G= NP_000425.1:n.353-113G=
NM_000434.4:c.353-113G= MANE Select NP_000425.1:n.353-113G=
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