Canonical Allele Identifier: CA2678054014

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861639-C-CAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861641_31861642insAAAA , CM000668.2:g.31861641_31861642insAAAA	GRCh38
NC_000006.11:g.31829418_31829419insAAAA , CM000668.1:g.31829418_31829419insAAAA	GRCh37
NC_000006.10:g.31937397_31937398insAAAA	NCBI36
NG_008201.1:g.6293_6294insTTTT
NG_023058.1:g.22407_22408insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-190_353-189insTTTT MANE Select	ENSP00000364782.4:n.353-190_353-189insTTTT
ENST00000677054.1:n.840_841insTTTT
ENST00000677512.1:n.461-190_461-189insTTTT
ENST00000678869.1:n.461-190_461-189insTTTT
ENST00000375631.4:c.353-190_353-189insTTTT	ENSP00000364782.4:n.353-190_353-189insTTTT
ENST00000480384.1:n.382-190_382-189insTTTT
ENST00000491768.5:c.353-190_353-189insTTTT	ENSP00000433127.1:n.353-190_353-189insTTTT
ENST00000495807.1:n.731_732insTTTT
NM_000434.3:c.353-190_353-189insTTTT	NP_000425.1:n.353-190_353-189insTTTT
NM_000434.4:c.353-190_353-189insTTTT MANE Select	NP_000425.1:n.353-190_353-189insTTTT