Canonical Allele Identifier: CA1619342379
Gene: NEU1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861587T= , CM000668.2:g.31861587T= GRCh38
NC_000006.11:g.31829364T= , CM000668.1:g.31829364T= GRCh37
NC_000006.10:g.31937343T= NCBI36
NG_008201.1:g.6346A=
NG_023058.1:g.22460A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.353-137A= MANE Select ENSP00000364782.4:n.353-137A=
ENST00000677054.1:n.893A=
ENST00000677512.1:n.461-137A=
ENST00000678869.1:n.461-137A=
ENST00000375631.4:c.353-137A= ENSP00000364782.4:n.353-137A=
ENST00000480384.1:n.382-137A=
ENST00000491768.5:c.353-137A= ENSP00000433127.1:n.353-137A=
ENST00000495807.1:n.784A=
NM_000434.3:c.353-137A= NP_000425.1:n.353-137A=
NM_000434.4:c.353-137A= MANE Select NP_000425.1:n.353-137A=
Search 100 bp 5'
Search 100 bp 3'