Canonical Allele Identifier: CA449808578
Gene: NEU1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31829145A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31861368A>G , CM000668.2:g.31861368A>G GRCh38
NC_000006.11:g.31829145A>G , CM000668.1:g.31829145A>G GRCh37
NC_000006.10:g.31937124A>G NCBI36
NG_008201.1:g.6565T>C
NG_023058.1:g.22679T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375631.5:c.435T>C MANE Select ENSP00000364782.4:p.Asp145=
ENST00000677054.1:n.1112T>C
ENST00000677512.1:n.543T>C
ENST00000678869.1:n.543T>C
ENST00000375631.4:c.435T>C ENSP00000364782.4:p.Asp145=
ENST00000480384.1:n.464T>C
ENST00000491768.5:c.435T>C ENSP00000433127.1:p.Asp145=
ENST00000495807.1:n.1003T>C
NM_000434.3:c.435T>C NP_000425.1:p.Asp145=
NM_000434.4:c.435T>C MANE Select NP_000425.1:p.Asp145=
Search 100 bp 5'
Search 100 bp 3'