Canonical Allele Identifier: CA2678053993

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861611-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861616del , CM000668.2:g.31861616del	GRCh38
NC_000006.11:g.31829393del , CM000668.1:g.31829393del	GRCh37
NC_000006.10:g.31937372del	NCBI36
NG_008201.1:g.6321del
NG_023058.1:g.22435del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-162del MANE Select	ENSP00000364782.4:n.353-162del
ENST00000677054.1:n.868del
ENST00000677512.1:n.461-162del
ENST00000678869.1:n.461-162del
ENST00000375631.4:c.353-162del	ENSP00000364782.4:n.353-162del
ENST00000480384.1:n.382-162del
ENST00000491768.5:c.353-162del	ENSP00000433127.1:n.353-162del
ENST00000495807.1:n.759del
NM_000434.3:c.353-162del	NP_000425.1:n.353-162del
NM_000434.4:c.353-162del MANE Select	NP_000425.1:n.353-162del