Canonical Allele Identifier: CA1619342396
Gene: NEU1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861621A= , CM000668.2:g.31861621A= GRCh38
NC_000006.11:g.31829398A= , CM000668.1:g.31829398A= GRCh37
NC_000006.10:g.31937377A= NCBI36
NG_008201.1:g.6312T=
NG_023058.1:g.22426T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-171T= MANE Select ENSP00000364782.4:n.353-171T=
ENST00000677054.1:n.859T=
ENST00000677512.1:n.461-171T=
ENST00000678869.1:n.461-171T=
ENST00000375631.4:c.353-171T= ENSP00000364782.4:n.353-171T=
ENST00000480384.1:n.382-171T=
ENST00000491768.5:c.353-171T= ENSP00000433127.1:n.353-171T=
ENST00000495807.1:n.750T=
NM_000434.3:c.353-171T= NP_000425.1:n.353-171T=
NM_000434.4:c.353-171T= MANE Select NP_000425.1:n.353-171T=
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