Canonical Allele Identifier: CA449808183

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31827514A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859737A>G , CM000668.2:g.31859737A>G	GRCh38
NC_000006.11:g.31827514A>G , CM000668.1:g.31827514A>G	GRCh37
NC_000006.10:g.31935493A>G	NCBI36
NG_008201.1:g.8196T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1230T>C MANE Select	ENSP00000364782.4:p.Ser410=
ENST00000677054.1:n.2569T>C
ENST00000677512.1:n.1507T>C
ENST00000678869.1:n.1818T>C
ENST00000375631.4:c.1230T>C	ENSP00000364782.4:p.Ser410=
ENST00000480384.1:n.1529T>C
ENST00000491768.5:c.*340T>C	ENSP00000433127.1:n.*340T>C
ENST00000495807.1:n.2538T>C
NM_000434.3:c.1230T>C	NP_000425.1:p.Ser410=
NM_000434.4:c.1230T>C MANE Select	NP_000425.1:p.Ser410=