Canonical Allele Identifier: CA2678053413

Gene: NEU1

Linked Data

• gnomAD v4: 6-31859947-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859951dup , CM000668.2:g.31859951dup	GRCh38
NC_000006.11:g.31827728dup , CM000668.1:g.31827728dup	GRCh37
NC_000006.10:g.31935707dup	NCBI36
NG_008201.1:g.7985dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1022-3dup MANE Select	ENSP00000364782.4:n.1022-3dup
ENST00000677054.1:n.2358dup
ENST00000677512.1:n.1299-3dup
ENST00000678869.1:n.1610-3dup
ENST00000375631.4:c.1022-3dup	ENSP00000364782.4:n.1022-3dup
ENST00000480384.1:n.1318dup
ENST00000491768.5:c.*132-3dup	ENSP00000433127.1:n.*132-3dup
ENST00000495807.1:n.2330-3dup
NM_000434.3:c.1022-3dup	NP_000425.1:n.1022-3dup
NM_000434.4:c.1022-3dup MANE Select	NP_000425.1:n.1022-3dup