Canonical Allele Identifier: CA2842859727

Gene: NEU1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861137C>A , CM000668.2:g.31861137C>A	GRCh38
NC_000006.11:g.31828914C>A , CM000668.1:g.31828914C>A	GRCh37
NC_000006.10:g.31936893C>A	NCBI36
NG_008201.1:g.6796G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.615+51G>T MANE Select	ENSP00000364782.4:n.615+51G>T
ENST00000677054.1:n.1343G>T
ENST00000677512.1:n.723+51G>T
ENST00000678869.1:n.774G>T
ENST00000375631.4:c.615+51G>T	ENSP00000364782.4:n.615+51G>T
ENST00000480384.1:n.644+51G>T
ENST00000491768.5:c.615+51G>T	ENSP00000433127.1:n.615+51G>T
ENST00000495807.1:n.1234G>T
NM_000434.3:c.615+51G>T	NP_000425.1:n.615+51G>T
NM_000434.4:c.615+51G>T MANE Select	NP_000425.1:n.615+51G>T