Canonical Allele Identifier: CA1619342359

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861546_31861547delinsAG , CM000668.2:g.31861546_31861547delinsAG	GRCh38
NC_000006.11:g.31829323_31829324delinsAG , CM000668.1:g.31829323_31829324delinsAG	GRCh37
NC_000006.10:g.31937302_31937303delinsAG	NCBI36
NG_008201.1:g.6386_6387delinsCT
NG_023058.1:g.22500_22501delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-97_353-96delinsCT MANE Select	ENSP00000364782.4:n.353-97_353-96delinsCT
ENST00000677054.1:n.933_934delinsCT
ENST00000677512.1:n.461-97_461-96delinsCT
ENST00000678869.1:n.461-97_461-96delinsCT
ENST00000375631.4:c.353-97_353-96delinsCT	ENSP00000364782.4:n.353-97_353-96delinsCT
ENST00000480384.1:n.382-97_382-96delinsCT
ENST00000491768.5:c.353-97_353-96delinsCT	ENSP00000433127.1:n.353-97_353-96delinsCT
ENST00000495807.1:n.824_825delinsCT
NM_000434.3:c.353-97_353-96delinsCT	NP_000425.1:n.353-97_353-96delinsCT
NM_000434.4:c.353-97_353-96delinsCT MANE Select	NP_000425.1:n.353-97_353-96delinsCT