Canonical Allele Identifier: CA1619341607
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1762425959
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859689G>A , CM000668.2:g.31859689G>A GRCh38
NC_000006.11:g.31827466G>A , CM000668.1:g.31827466G>A GRCh37
NC_000006.10:g.31935445G>A NCBI36
NG_008201.1:g.8244C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.*30C>T MANE Select ENSP00000364782.4:n.*30C>T
ENST00000677054.1:n.2617C>T
ENST00000677512.1:n.1555C>T
ENST00000678869.1:n.1866C>T
ENST00000375631.4:c.*30C>T ENSP00000364782.4:n.*30C>T
ENST00000480384.1:n.1577C>T
ENST00000491768.5:c.*388C>T ENSP00000433127.1:n.*388C>T
ENST00000495807.1:n.2586C>T
NM_000434.3:c.*30C>T NP_000425.1:n.*30C>T
NM_000434.4:c.*30C>T MANE Select NP_000425.1:n.*30C>T
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