Canonical Allele Identifier: CA1619341593
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859657C= , CM000668.2:g.31859657C= GRCh38
NC_000006.11:g.31827434C= , CM000668.1:g.31827434C= GRCh37
NC_000006.10:g.31935413C= NCBI36
NG_008201.1:g.8276G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*62G= MANE Select ENSP00000364782.4:n.*62G=
ENST00000677054.1:n.2649G=
ENST00000677512.1:n.1587G=
ENST00000678869.1:n.1898G=
ENST00000375631.4:c.*62G= ENSP00000364782.4:n.*62G=
ENST00000480384.1:n.1609G=
ENST00000491768.5:c.*420G= ENSP00000433127.1:n.*420G=
ENST00000495807.1:n.2618G=
NM_000434.3:c.*62G= NP_000425.1:n.*62G=
NM_000434.4:c.*62G= MANE Select NP_000425.1:n.*62G=
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