Canonical Allele Identifier: CA363486241
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827716T>C (hg19) chr6:g.31859939T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859939T>C , CM000668.2:g.31859939T>C GRCh38
NC_000006.11:g.31827716T>C , CM000668.1:g.31827716T>C GRCh37
NC_000006.10:g.31935695T>C NCBI36
NG_008201.1:g.7994A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.1028A>G MANE Select ENSP00000364782.4:p.Asn343Ser
ENST00000677054.1:n.2367A>G
ENST00000677512.1:n.1305A>G
ENST00000678869.1:n.1616A>G
ENST00000375631.4:c.1028A>G ENSP00000364782.4:p.Asn343Ser
ENST00000480384.1:n.1327A>G
ENST00000491768.5:c.*138A>G ENSP00000433127.1:n.*138A>G
ENST00000495807.1:n.2336A>G
NM_000434.3:c.1028A>G NP_000425.1:p.Asn343Ser
NM_000434.4:c.1028A>G MANE Select NP_000425.1:p.Asn343Ser
Search 100 bp 5'
Search 100 bp 3'