Canonical Allele Identifier: CA1619342367

Gene: NEU1

Linked Data

• dbSNP Id: rs1762514947

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861565G>C , CM000668.2:g.31861565G>C	GRCh38
NC_000006.11:g.31829342G>C , CM000668.1:g.31829342G>C	GRCh37
NC_000006.10:g.31937321G>C	NCBI36
NG_008201.1:g.6368C>G
NG_023058.1:g.22482C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-115C>G MANE Select	ENSP00000364782.4:n.353-115C>G
ENST00000677054.1:n.915C>G
ENST00000677512.1:n.461-115C>G
ENST00000678869.1:n.461-115C>G
ENST00000375631.4:c.353-115C>G	ENSP00000364782.4:n.353-115C>G
ENST00000480384.1:n.382-115C>G
ENST00000491768.5:c.353-115C>G	ENSP00000433127.1:n.353-115C>G
ENST00000495807.1:n.806C>G
NM_000434.3:c.353-115C>G	NP_000425.1:n.353-115C>G
NM_000434.4:c.353-115C>G MANE Select	NP_000425.1:n.353-115C>G