Canonical Allele Identifier: CA823920875

Gene: NEU1

Linked Data

• dbSNP Id: rs1412305117
• MyVariant Identifiers: chr6:g.31829418_31829419del (hg19) ; chr6:g.31861641_31861642del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861642_31861643del , CM000668.2:g.31861642_31861643del	GRCh38
NC_000006.11:g.31829419_31829420del , CM000668.1:g.31829419_31829420del	GRCh37
NC_000006.10:g.31937398_31937399del	NCBI36
NG_008201.1:g.6291_6292del
NG_023058.1:g.22405_22406del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-192_353-191del MANE Select	ENSP00000364782.4:n.353-192_353-191del
ENST00000677054.1:n.838_839del
ENST00000677512.1:n.461-192_461-191del
ENST00000678869.1:n.461-192_461-191del
ENST00000375631.4:c.353-192_353-191del	ENSP00000364782.4:n.353-192_353-191del
ENST00000480384.1:n.382-192_382-191del
ENST00000491768.5:c.353-192_353-191del	ENSP00000433127.1:n.353-192_353-191del
ENST00000495807.1:n.729_730del
NM_000434.3:c.353-192_353-191del	NP_000425.1:n.353-192_353-191del
NM_000434.4:c.353-192_353-191del MANE Select	NP_000425.1:n.353-192_353-191del