Canonical Allele Identifier: CA363486392
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827723C>T (hg19) chr6:g.31859946C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859946C>T , CM000668.2:g.31859946C>T GRCh38
NC_000006.11:g.31827723C>T , CM000668.1:g.31827723C>T GRCh37
NC_000006.10:g.31935702C>T NCBI36
NG_008201.1:g.7987G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.1022-1G>A MANE Select ENSP00000364782.4:n.1022-1G>A
ENST00000677054.1:n.2360G>A
ENST00000677512.1:n.1299-1G>A
ENST00000678869.1:n.1610-1G>A
ENST00000375631.4:c.1022-1G>A ENSP00000364782.4:n.1022-1G>A
ENST00000480384.1:n.1320G>A
ENST00000491768.5:c.*132-1G>A ENSP00000433127.1:n.*132-1G>A
ENST00000495807.1:n.2330-1G>A
NM_000434.3:c.1022-1G>A NP_000425.1:n.1022-1G>A
NM_000434.4:c.1022-1G>A MANE Select NP_000425.1:n.1022-1G>A
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