Canonical Allele Identifier: CA363486739
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31827827G>C (hg19) chr6:g.31860050G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860050G>C , CM000668.2:g.31860050G>C GRCh38
NC_000006.11:g.31827827G>C , CM000668.1:g.31827827G>C GRCh37
NC_000006.10:g.31935806G>C NCBI36
NG_008201.1:g.7883C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.1013C>G MANE Select ENSP00000364782.4:p.Pro338Arg
ENST00000677054.1:n.2256C>G
ENST00000677512.1:n.1295C>G
ENST00000678869.1:n.1601C>G
ENST00000375631.4:c.1013C>G ENSP00000364782.4:p.Pro338Arg
ENST00000480384.1:n.1216C>G
ENST00000491768.5:c.*123C>G ENSP00000433127.1:n.*123C>G
ENST00000495807.1:n.2321C>G
NM_000434.3:c.1013C>G NP_000425.1:p.Pro338Arg
NM_000434.4:c.1013C>G MANE Select NP_000425.1:p.Pro338Arg
Search 100 bp 5'
Search 100 bp 3'