Canonical Allele Identifier: CA384387380
Gene: ALG10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.34179768T>A (hg19) chr12:g.34026833T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.34026833T>A , CM000674.2:g.34026833T>A GRCh38
NC_000012.11:g.34179768T>A , CM000674.1:g.34179768T>A GRCh37
NC_000012.10:g.34071035T>A NCBI36
NG_016389.1:g.9553T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000266483.7:c.1340T>A MANE Select ENSP00000266483.2:p.Val447Asp
ENST00000266483.6:c.1340T>A ENSP00000266483.2:p.Val447Asp
ENST00000538927.1:c.369+2674T>A ENSP00000444084.1:n.369+2674T>A
ENST00000541875.1:c.*1080T>A ENSP00000443142.1:n.*1080T>A
NM_032834.3:c.1340T>A NP_116223.3:p.Val447Asp
XM_024449230.1:c.1160T>A XP_024304998.1:p.Val387Asp
XM_024449231.1:c.1160T>A XP_024304999.1:p.Val387Asp
NM_032834.4:c.1340T>A MANE Select NP_116223.3:p.Val447Asp
Search 100 bp 5'
Search 100 bp 3'