Canonical Allele Identifier: CA136926063
Gene: NEU1 HGNC NCBI

Linked Data

dbSNP Id: rs866082815
MyVariant Identifiers: chr6:g.31828246_31828247insCT (hg19) chr6:g.31860469_31860470insCT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31860469_31860470insCT , CM000668.2:g.31860469_31860470insCT GRCh38
NC_000006.11:g.31828246_31828247insCT , CM000668.1:g.31828246_31828247insCT GRCh37
NC_000006.10:g.31936225_31936226insCT NCBI36
NG_008201.1:g.7463_7464insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.767_768insAG MANE Select ENSP00000364782.4:p.Glu257GlyfsTer?
ENST00000677054.1:n.2010_2011insAG
ENST00000677512.1:n.875_876insAG
ENST00000678869.1:n.1441_1442insAG
ENST00000375631.4:c.767_768insAG ENSP00000364782.4:p.Glu257GlyfsTer?
ENST00000480384.1:n.796_797insAG
ENST00000491768.5:c.767_768insAG ENSP00000433127.1:p.Glu257GlyfsTer?
ENST00000495807.1:n.1901_1902insAG
NM_000434.3:c.767_768insAG NP_000425.1:p.Glu257GlyfsTer?
NM_000434.4:c.767_768insAG MANE Select NP_000425.1:p.Glu257GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'