Canonical Allele Identifier: CA363486399
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827724T>A (hg19) chr6:g.31859947T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859947T>A , CM000668.2:g.31859947T>A GRCh38
NC_000006.11:g.31827724T>A , CM000668.1:g.31827724T>A GRCh37
NC_000006.10:g.31935703T>A NCBI36
NG_008201.1:g.7986A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.1022-2A>T MANE Select ENSP00000364782.4:n.1022-2A>T
ENST00000677054.1:n.2359A>T
ENST00000677512.1:n.1299-2A>T
ENST00000678869.1:n.1610-2A>T
ENST00000375631.4:c.1022-2A>T ENSP00000364782.4:n.1022-2A>T
ENST00000480384.1:n.1319A>T
ENST00000491768.5:c.*132-2A>T ENSP00000433127.1:n.*132-2A>T
ENST00000495807.1:n.2330-2A>T
NM_000434.3:c.1022-2A>T NP_000425.1:n.1022-2A>T
NM_000434.4:c.1022-2A>T MANE Select NP_000425.1:n.1022-2A>T
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