Canonical Allele Identifier: CA479228638
Gene: ALG10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.34179781T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.34026846T>G , CM000674.2:g.34026846T>G GRCh38
NC_000012.11:g.34179781T>G , CM000674.1:g.34179781T>G GRCh37
NC_000012.10:g.34071048T>G NCBI36
NG_016389.1:g.9566T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000266483.7:c.1353T>G MANE Select ENSP00000266483.2:p.Thr451=
ENST00000266483.6:c.1353T>G ENSP00000266483.2:p.Thr451=
ENST00000538927.1:c.369+2687T>G ENSP00000444084.1:n.369+2687T>G
ENST00000541875.1:c.*1093T>G ENSP00000443142.1:n.*1093T>G
NM_032834.3:c.1353T>G NP_116223.3:p.Thr451=
XM_024449230.1:c.1173T>G XP_024304998.1:p.Thr391=
XM_024449231.1:c.1173T>G XP_024304999.1:p.Thr391=
NM_032834.4:c.1353T>G MANE Select NP_116223.3:p.Thr451=
Search 100 bp 5'
Search 100 bp 3'