Canonical Allele Identifier: CA2678053422

Gene: NEU1

Linked Data

• gnomAD v4: 6-31859965-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859966dup , CM000668.2:g.31859966dup	GRCh38
NC_000006.11:g.31827743dup , CM000668.1:g.31827743dup	GRCh37
NC_000006.10:g.31935722dup	NCBI36
NG_008201.1:g.7967dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1022-21dup MANE Select	ENSP00000364782.4:n.1022-21dup
ENST00000677054.1:n.2340dup
ENST00000677512.1:n.1299-21dup
ENST00000678869.1:n.1610-21dup
ENST00000375631.4:c.1022-21dup	ENSP00000364782.4:n.1022-21dup
ENST00000480384.1:n.1300dup
ENST00000491768.5:c.*132-21dup	ENSP00000433127.1:n.*132-21dup
ENST00000495807.1:n.2330-21dup
NM_000434.3:c.1022-21dup	NP_000425.1:n.1022-21dup
NM_000434.4:c.1022-21dup MANE Select	NP_000425.1:n.1022-21dup