Canonical Allele Identifier: CA1619342392
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861617C= , CM000668.2:g.31861617C= GRCh38
NC_000006.11:g.31829394C= , CM000668.1:g.31829394C= GRCh37
NC_000006.10:g.31937373C= NCBI36
NG_008201.1:g.6316G=
NG_023058.1:g.22430G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-167G= MANE Select ENSP00000364782.4:n.353-167G=
ENST00000677054.1:n.863G=
ENST00000677512.1:n.461-167G=
ENST00000678869.1:n.461-167G=
ENST00000375631.4:c.353-167G= ENSP00000364782.4:n.353-167G=
ENST00000480384.1:n.382-167G=
ENST00000491768.5:c.353-167G= ENSP00000433127.1:n.353-167G=
ENST00000495807.1:n.754G=
NM_000434.3:c.353-167G= NP_000425.1:n.353-167G=
NM_000434.4:c.353-167G= MANE Select NP_000425.1:n.353-167G=
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