Canonical Allele Identifier: CA363486754

Gene: NEU1

Linked Data

• MyVariant Identifiers: chr6:g.31827828G>T (hg19) ; chr6:g.31860051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31860051G>T , CM000668.2:g.31860051G>T	GRCh38
NC_000006.11:g.31827828G>T , CM000668.1:g.31827828G>T	GRCh37
NC_000006.10:g.31935807G>T	NCBI36
NG_008201.1:g.7882C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.1012C>A MANE Select	ENSP00000364782.4:p.Pro338Thr
ENST00000677054.1:n.2255C>A
ENST00000677512.1:n.1294C>A
ENST00000678869.1:n.1600C>A
ENST00000375631.4:c.1012C>A	ENSP00000364782.4:p.Pro338Thr
ENST00000480384.1:n.1215C>A
ENST00000491768.5:c.*122C>A	ENSP00000433127.1:n.*122C>A
ENST00000495807.1:n.2320C>A
NM_000434.3:c.1012C>A	NP_000425.1:p.Pro338Thr
NM_000434.4:c.1012C>A MANE Select	NP_000425.1:p.Pro338Thr