Canonical Allele Identifier: CA363494909
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31829168T>C (hg19) chr6:g.31861391T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861391T>C , CM000668.2:g.31861391T>C GRCh38
NC_000006.11:g.31829168T>C , CM000668.1:g.31829168T>C GRCh37
NC_000006.10:g.31937147T>C NCBI36
NG_008201.1:g.6542A>G
NG_023058.1:g.22656A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.412A>G MANE Select ENSP00000364782.4:p.Asn138Asp
ENST00000677054.1:n.1089A>G
ENST00000677512.1:n.520A>G
ENST00000678869.1:n.520A>G
ENST00000375631.4:c.412A>G ENSP00000364782.4:p.Asn138Asp
ENST00000480384.1:n.441A>G
ENST00000491768.5:c.412A>G ENSP00000433127.1:p.Asn138Asp
ENST00000495807.1:n.980A>G
NM_000434.3:c.412A>G NP_000425.1:p.Asn138Asp
NM_000434.4:c.412A>G MANE Select NP_000425.1:p.Asn138Asp
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Search 100 bp 3'