Canonical Allele Identifier: CA1619342293
Gene: NEU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861381G= , CM000668.2:g.31861381G= GRCh38
NC_000006.11:g.31829158G= , CM000668.1:g.31829158G= GRCh37
NC_000006.10:g.31937137G= NCBI36
NG_008201.1:g.6552C=
NG_023058.1:g.22666C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.422C= MANE Select ENSP00000364782.4:p.Ala141=
ENST00000677054.1:n.1099C=
ENST00000677512.1:n.530C=
ENST00000678869.1:n.530C=
ENST00000375631.4:c.422C= ENSP00000364782.4:p.Ala141=
ENST00000480384.1:n.451C=
ENST00000491768.5:c.422C= ENSP00000433127.1:p.Ala141=
ENST00000495807.1:n.990C=
NM_000434.3:c.422C= NP_000425.1:p.Ala141=
NM_000434.4:c.422C= MANE Select NP_000425.1:p.Ala141=