Canonical Allele Identifier: CA1619341621

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859732_31859737delinsTAGACA , CM000668.2:g.31859732_31859737delinsTAGACA	GRCh38
NC_000006.11:g.31827509_31827514delinsTAGACA , CM000668.1:g.31827509_31827514delinsTAGACA	GRCh37
NC_000006.10:g.31935488_31935493delinsTAGACA	NCBI36
NG_008201.1:g.8196_8201delinsTGTCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1230_1235delinsTGTCTA MANE Select	ENSP00000364782.4:p.Ser410=
ENST00000677054.1:n.2569_2574delinsTGTCTA
ENST00000677512.1:n.1507_1512delinsTGTCTA
ENST00000678869.1:n.1818_1823delinsTGTCTA
ENST00000375631.4:c.1230_1235delinsTGTCTA	ENSP00000364782.4:p.Ser410=
ENST00000480384.1:n.1529_1534delinsTGTCTA
ENST00000491768.5:c.*340_*345delinsTGTCTA	ENSP00000433127.1:n.*340_*345delinsTGTCTA...
ENST00000495807.1:n.2538_2543delinsTGTCTA
NM_000434.3:c.1230_1235delinsTGTCTA	NP_000425.1:p.Ser410=
NM_000434.4:c.1230_1235delinsTGTCTA MANE Select	NP_000425.1:p.Ser410=