Canonical Allele Identifier: CA1619342381

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861588_31861590delinsATC , CM000668.2:g.31861588_31861590delinsATC	GRCh38
NC_000006.11:g.31829365_31829367delinsATC , CM000668.1:g.31829365_31829367delinsATC	GRCh37
NC_000006.10:g.31937344_31937346delinsATC	NCBI36
NG_008201.1:g.6343_6345delinsGAT
NG_023058.1:g.22457_22459delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-140_353-138delinsGAT MANE Select	ENSP00000364782.4:n.353-140_353-138delinsGAT
ENST00000677054.1:n.890_892delinsGAT
ENST00000677512.1:n.461-140_461-138delinsGAT
ENST00000678869.1:n.461-140_461-138delinsGAT
ENST00000375631.4:c.353-140_353-138delinsGAT	ENSP00000364782.4:n.353-140_353-138delinsGAT
ENST00000480384.1:n.382-140_382-138delinsGAT
ENST00000491768.5:c.353-140_353-138delinsGAT	ENSP00000433127.1:n.353-140_353-138delinsGAT
ENST00000495807.1:n.781_783delinsGAT
NM_000434.3:c.353-140_353-138delinsGAT	NP_000425.1:n.353-140_353-138delinsGAT
NM_000434.4:c.353-140_353-138delinsGAT MANE Select	NP_000425.1:n.353-140_353-138delinsGAT