Canonical Allele Identifier: CA363492244

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31828296A>T (hg19) ; chr6:g.31860519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860519A>T , CM000668.2:g.31860519A>T	GRCh38
NC_000006.11:g.31828296A>T , CM000668.1:g.31828296A>T	GRCh37
NC_000006.10:g.31936275A>T	NCBI36
NG_008201.1:g.7414T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375631.5:c.718T>A MANE Select	ENSP00000364782.4:p.Trp240Arg
ENST00000677054.1:n.1961T>A
ENST00000677512.1:n.826T>A
ENST00000678869.1:n.1392T>A
ENST00000375631.4:c.718T>A	ENSP00000364782.4:p.Trp240Arg
ENST00000480384.1:n.747T>A
ENST00000491768.5:c.718T>A	ENSP00000433127.1:p.Trp240Arg
ENST00000495807.1:n.1852T>A
NM_000434.3:c.718T>A	NP_000425.1:p.Trp240Arg
NM_000434.4:c.718T>A MANE Select	NP_000425.1:p.Trp240Arg