Canonical Allele Identifier: CA449675024
Gene: NEU1 HGNC NCBI

Linked Data

gnomAD v4: 6-31862024-G-A
MyVariant Identifiers: chr6:g.31829801G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31862024G>A , CM000668.2:g.31862024G>A GRCh38
NC_000006.11:g.31829801G>A , CM000668.1:g.31829801G>A GRCh37
NC_000006.10:g.31937780G>A NCBI36
NG_008201.1:g.5909C>T
NG_023058.1:g.22023C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000375631.5:c.327C>T MANE Select ENSP00000364782.4:p.Ile109=
ENST00000677054.1:n.456C>T
ENST00000677512.1:n.435C>T
ENST00000678869.1:n.435C>T
ENST00000375631.4:c.327C>T ENSP00000364782.4:p.Ile109=
ENST00000480384.1:n.356C>T
ENST00000491768.5:c.327C>T ENSP00000433127.1:p.Ile109=
ENST00000495807.1:n.347C>T
NM_000434.3:c.327C>T NP_000425.1:p.Ile109=
NM_000434.4:c.327C>T MANE Select NP_000425.1:p.Ile109=