Canonical Allele Identifier: CA2842859726

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861131dup , CM000668.2:g.31861131dup	GRCh38
NC_000006.11:g.31828908dup , CM000668.1:g.31828908dup	GRCh37
NC_000006.10:g.31936887dup	NCBI36
NG_008201.1:g.6806dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.615+61dup MANE Select	ENSP00000364782.4:n.615+61dup
ENST00000677054.1:n.1353dup
ENST00000677512.1:n.723+61dup
ENST00000678869.1:n.784dup
ENST00000375631.4:c.615+61dup	ENSP00000364782.4:n.615+61dup
ENST00000480384.1:n.644+61dup
ENST00000491768.5:c.615+61dup	ENSP00000433127.1:n.615+61dup
ENST00000495807.1:n.1244dup
NM_000434.3:c.615+61dup	NP_000425.1:n.615+61dup
NM_000434.4:c.615+61dup MANE Select	NP_000425.1:n.615+61dup