Canonical Allele Identifier: CA1619341606
Gene: NEU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31859689G= , CM000668.2:g.31859689G= GRCh38
NC_000006.11:g.31827466G= , CM000668.1:g.31827466G= GRCh37
NC_000006.10:g.31935445G= NCBI36
NG_008201.1:g.8244C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.*30C= MANE Select ENSP00000364782.4:n.*30C=
ENST00000677054.1:n.2617C=
ENST00000677512.1:n.1555C=
ENST00000678869.1:n.1866C=
ENST00000375631.4:c.*30C= ENSP00000364782.4:n.*30C=
ENST00000480384.1:n.1577C=
ENST00000491768.5:c.*388C= ENSP00000433127.1:n.*388C=
ENST00000495807.1:n.2586C=
NM_000434.3:c.*30C= NP_000425.1:n.*30C=
NM_000434.4:c.*30C= MANE Select NP_000425.1:n.*30C=