Canonical Allele Identifier: CA1619342559
Gene: NEU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31862014T= , CM000668.2:g.31862014T= GRCh38
NC_000006.11:g.31829791T= , CM000668.1:g.31829791T= GRCh37
NC_000006.10:g.31937770T= NCBI36
NG_008201.1:g.5919A=
NG_023058.1:g.22033A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.337A= MANE Select ENSP00000364782.4:p.Arg113=
ENST00000677054.1:n.466A=
ENST00000677512.1:n.445A=
ENST00000678869.1:n.445A=
ENST00000375631.4:c.337A= ENSP00000364782.4:p.Arg113=
ENST00000480384.1:n.366A=
ENST00000491768.5:c.337A= ENSP00000433127.1:p.Arg113=
ENST00000495807.1:n.357A=
NM_000434.3:c.337A= NP_000425.1:p.Arg113=
NM_000434.4:c.337A= MANE Select NP_000425.1:p.Arg113=