Canonical Allele Identifier: CA2678053975

Gene: NEU1

Linked Data

• gnomAD v4: 6-31861594-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31861594A>C , CM000668.2:g.31861594A>C	GRCh38
NC_000006.11:g.31829371A>C , CM000668.1:g.31829371A>C	GRCh37
NC_000006.10:g.31937350A>C	NCBI36
NG_008201.1:g.6339T>G
NG_023058.1:g.22453T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375631.5:c.353-144T>G MANE Select	ENSP00000364782.4:n.353-144T>G
ENST00000677054.1:n.886T>G
ENST00000677512.1:n.461-144T>G
ENST00000678869.1:n.461-144T>G
ENST00000375631.4:c.353-144T>G	ENSP00000364782.4:n.353-144T>G
ENST00000480384.1:n.382-144T>G
ENST00000491768.5:c.353-144T>G	ENSP00000433127.1:n.353-144T>G
ENST00000495807.1:n.777T>G
NM_000434.3:c.353-144T>G	NP_000425.1:n.353-144T>G
NM_000434.4:c.353-144T>G MANE Select	NP_000425.1:n.353-144T>G