Canonical Allele Identifier: CA363495513
Gene: NEU1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.337A>T MANE Select ENSP00000364782.4:p.Arg113Trp
ENST00000677054.1:n.466A>T
ENST00000677512.1:n.445A>T
ENST00000678869.1:n.445A>T
ENST00000375631.4:c.337A>T ENSP00000364782.4:p.Arg113Trp
ENST00000480384.1:n.366A>T
ENST00000491768.5:c.337A>T ENSP00000433127.1:p.Arg113Trp
ENST00000495807.1:n.357A>T
NM_000434.3:c.337A>T NP_000425.1:p.Arg113Trp
NM_000434.4:c.337A>T MANE Select NP_000425.1:p.Arg113Trp