Canonical Allele Identifier: CA1619342397
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861622T= , CM000668.2:g.31861622T= GRCh38
NC_000006.11:g.31829399T= , CM000668.1:g.31829399T= GRCh37
NC_000006.10:g.31937378T= NCBI36
NG_008201.1:g.6311A=
NG_023058.1:g.22425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-172A= MANE Select ENSP00000364782.4:n.353-172A=
ENST00000677054.1:n.858A=
ENST00000677512.1:n.461-172A=
ENST00000678869.1:n.461-172A=
ENST00000375631.4:c.353-172A= ENSP00000364782.4:n.353-172A=
ENST00000480384.1:n.382-172A=
ENST00000491768.5:c.353-172A= ENSP00000433127.1:n.353-172A=
ENST00000495807.1:n.749A=
NM_000434.3:c.353-172A= NP_000425.1:n.353-172A=
NM_000434.4:c.353-172A= MANE Select NP_000425.1:n.353-172A=
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