Canonical Allele Identifier: CA2842859728

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861154dup , CM000668.2:g.31861154dup	GRCh38
NC_000006.11:g.31828931dup , CM000668.1:g.31828931dup	GRCh37
NC_000006.10:g.31936910dup	NCBI36
NG_008201.1:g.6780dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.615+35dup MANE Select	ENSP00000364782.4:n.615+35dup
ENST00000677054.1:n.1327dup
ENST00000677512.1:n.723+35dup
ENST00000678869.1:n.758dup
ENST00000375631.4:c.615+35dup	ENSP00000364782.4:n.615+35dup
ENST00000480384.1:n.644+35dup
ENST00000491768.5:c.615+35dup	ENSP00000433127.1:n.615+35dup
ENST00000495807.1:n.1218dup
NM_000434.3:c.615+35dup	NP_000425.1:n.615+35dup
NM_000434.4:c.615+35dup MANE Select	NP_000425.1:n.615+35dup