Canonical Allele Identifier: CA2678053960

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861572-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861572_31861573insG , CM000668.2:g.31861572_31861573insG	GRCh38
NC_000006.11:g.31829349_31829350insG , CM000668.1:g.31829349_31829350insG	GRCh37
NC_000006.10:g.31937328_31937329insG	NCBI36
NG_008201.1:g.6360_6361insC
NG_023058.1:g.22474_22475insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-123_353-122insC MANE Select	ENSP00000364782.4:n.353-123_353-122insC
ENST00000677054.1:n.907_908insC
ENST00000677512.1:n.461-123_461-122insC
ENST00000678869.1:n.461-123_461-122insC
ENST00000375631.4:c.353-123_353-122insC	ENSP00000364782.4:n.353-123_353-122insC
ENST00000480384.1:n.382-123_382-122insC
ENST00000491768.5:c.353-123_353-122insC	ENSP00000433127.1:n.353-123_353-122insC
ENST00000495807.1:n.798_799insC
NM_000434.3:c.353-123_353-122insC	NP_000425.1:n.353-123_353-122insC
NM_000434.4:c.353-123_353-122insC MANE Select	NP_000425.1:n.353-123_353-122insC