Canonical Allele Identifier: CA1619341605
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs1762425857
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859688A>G , CM000668.2:g.31859688A>G GRCh38
NC_000006.11:g.31827465A>G , CM000668.1:g.31827465A>G GRCh37
NC_000006.10:g.31935444A>G NCBI36
NG_008201.1:g.8245T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*31T>C MANE Select ENSP00000364782.4:n.*31T>C
ENST00000677054.1:n.2618T>C
ENST00000677512.1:n.1556T>C
ENST00000678869.1:n.1867T>C
ENST00000375631.4:c.*31T>C ENSP00000364782.4:n.*31T>C
ENST00000480384.1:n.1578T>C
ENST00000491768.5:c.*389T>C ENSP00000433127.1:n.*389T>C
ENST00000495807.1:n.2587T>C
NM_000434.3:c.*31T>C NP_000425.1:n.*31T>C
NM_000434.4:c.*31T>C MANE Select NP_000425.1:n.*31T>C
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