Canonical Allele Identifier: CA1619342290
Gene: NEU1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861375A= , CM000668.2:g.31861375A= GRCh38
NC_000006.11:g.31829152A= , CM000668.1:g.31829152A= GRCh37
NC_000006.10:g.31937131A= NCBI36
NG_008201.1:g.6558T=
NG_023058.1:g.22672T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.428T= MANE Select ENSP00000364782.4:p.Val143=
ENST00000677054.1:n.1105T=
ENST00000677512.1:n.536T=
ENST00000678869.1:n.536T=
ENST00000375631.4:c.428T= ENSP00000364782.4:p.Val143=
ENST00000480384.1:n.457T=
ENST00000491768.5:c.428T= ENSP00000433127.1:p.Val143=
ENST00000495807.1:n.996T=
NM_000434.3:c.428T= NP_000425.1:p.Val143=
NM_000434.4:c.428T= MANE Select NP_000425.1:p.Val143=