Canonical Allele Identifier: CA1619341716

Gene: NEU1

Linked Data

• dbSNP Id: rs1762438781

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859959G>A , CM000668.2:g.31859959G>A	GRCh38
NC_000006.11:g.31827736G>A , CM000668.1:g.31827736G>A	GRCh37
NC_000006.10:g.31935715G>A	NCBI36
NG_008201.1:g.7974C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1022-14C>T MANE Select	ENSP00000364782.4:n.1022-14C>T
ENST00000677054.1:n.2347C>T
ENST00000677512.1:n.1299-14C>T
ENST00000678869.1:n.1610-14C>T
ENST00000375631.4:c.1022-14C>T	ENSP00000364782.4:n.1022-14C>T
ENST00000480384.1:n.1307C>T
ENST00000491768.5:c.*132-14C>T	ENSP00000433127.1:n.*132-14C>T
ENST00000495807.1:n.2330-14C>T
NM_000434.3:c.1022-14C>T	NP_000425.1:n.1022-14C>T
NM_000434.4:c.1022-14C>T MANE Select	NP_000425.1:n.1022-14C>T