Canonical Allele Identifier: CA384387396

Gene: ALG10

Linked Data

• MyVariant Identifiers: chr12:g.34179771A>T (hg19) ; chr12:g.34026836A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.34026836A>T , CM000674.2:g.34026836A>T	GRCh38
NC_000012.11:g.34179771A>T , CM000674.1:g.34179771A>T	GRCh37
NC_000012.10:g.34071038A>T	NCBI36
NG_016389.1:g.9556A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266483.7:c.1343A>T MANE Select	ENSP00000266483.2:p.Asn448Ile
ENST00000266483.6:c.1343A>T	ENSP00000266483.2:p.Asn448Ile
ENST00000538927.1:c.369+2677A>T	ENSP00000444084.1:n.369+2677A>T
ENST00000541875.1:c.*1083A>T	ENSP00000443142.1:n.*1083A>T
NM_032834.3:c.1343A>T	NP_116223.3:p.Asn448Ile
XM_024449230.1:c.1163A>T	XP_024304998.1:p.Asn388Ile
XM_024449231.1:c.1163A>T	XP_024304999.1:p.Asn388Ile
NM_032834.4:c.1343A>T MANE Select	NP_116223.3:p.Asn448Ile