Canonical Allele Identifier: CA449808216

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31827529G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31859752G>T , CM000668.2:g.31859752G>T	GRCh38
NC_000006.11:g.31827529G>T , CM000668.1:g.31827529G>T	GRCh37
NC_000006.10:g.31935508G>T	NCBI36
NG_008201.1:g.8181C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.1215C>A MANE Select	ENSP00000364782.4:p.Ser405=
ENST00000677054.1:n.2554C>A
ENST00000677512.1:n.1492C>A
ENST00000678869.1:n.1803C>A
ENST00000375631.4:c.1215C>A	ENSP00000364782.4:p.Ser405=
ENST00000480384.1:n.1514C>A
ENST00000491768.5:c.*325C>A	ENSP00000433127.1:n.*325C>A
ENST00000495807.1:n.2523C>A
NM_000434.3:c.1215C>A	NP_000425.1:p.Ser405=
NM_000434.4:c.1215C>A MANE Select	NP_000425.1:p.Ser405=