Canonical Allele Identifier: CA917713202

Gene: NEU1

Linked Data

• dbSNP Id: rs1562433003

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861179_31861183del , CM000668.2:g.31861179_31861183del	GRCh38
NC_000006.11:g.31828956_31828960del , CM000668.1:g.31828956_31828960del	GRCh37
NC_000006.10:g.31936935_31936939del	NCBI36
NG_008201.1:g.6752_6756del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.615+7_615+11del MANE Select	ENSP00000364782.4:n.615+7_615+11del
ENST00000677054.1:n.1299_1303del
ENST00000677512.1:n.723+7_723+11del
ENST00000678869.1:n.730_734del
ENST00000375631.4:c.615+7_615+11del	ENSP00000364782.4:n.615+7_615+11del
ENST00000480384.1:n.644+7_644+11del
ENST00000491768.5:c.615+7_615+11del	ENSP00000433127.1:n.615+7_615+11del
ENST00000495807.1:n.1190_1194del
NM_000434.3:c.615+7_615+11del	NP_000425.1:n.615+7_615+11del
NM_000434.4:c.615+7_615+11del MANE Select	NP_000425.1:n.615+7_615+11del