Canonical Allele Identifier: CA363495209
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31829219A>C (hg19) chr6:g.31861442A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861442A>C , CM000668.2:g.31861442A>C GRCh38
NC_000006.11:g.31829219A>C , CM000668.1:g.31829219A>C GRCh37
NC_000006.10:g.31937198A>C NCBI36
NG_008201.1:g.6491T>G
NG_023058.1:g.22605T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.361T>G MANE Select ENSP00000364782.4:p.Trp121Gly
ENST00000677054.1:n.1038T>G
ENST00000677512.1:n.469T>G
ENST00000678869.1:n.469T>G
ENST00000375631.4:c.361T>G ENSP00000364782.4:p.Trp121Gly
ENST00000480384.1:n.390T>G
ENST00000491768.5:c.361T>G ENSP00000433127.1:p.Trp121Gly
ENST00000495807.1:n.929T>G
NM_000434.3:c.361T>G NP_000425.1:p.Trp121Gly
NM_000434.4:c.361T>G MANE Select NP_000425.1:p.Trp121Gly
Search 100 bp 5'
Search 100 bp 3'