Canonical Allele Identifier: CA341748770

Gene: AMPD1

Linked Data

• dbSNP Id: rs1399359392
• gnomAD v2: 1-115220135-C-T
• gnomAD v4: 1-114677514-C-T
• MyVariant Identifiers: chr1:g.115220135C>T (hg19) ; chr1:g.114677514C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677514C>T , CM000663.2:g.114677514C>T	GRCh38
NC_000001.10:g.115220135C>T , CM000663.1:g.115220135C>T	GRCh37
NC_000001.9:g.115021658C>T	NCBI36
NG_008012.1:g.23042G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1213G>A	ENSP00000358551.4:p.Glu405Lys
ENST00000520113.7:c.1225G>A MANE Select	ENSP00000430075.3:p.Glu409Lys
ENST00000637080.1:c.1008G>A	ENSP00000489753.1:n.1008G>A
ENST00000639077.1:n.890G>A
ENST00000369538.3:c.1312G>A	ENSP00000358551.3:p.Glu438Lys
ENST00000520113.6:c.1324G>A	ENSP00000430075.2:p.Glu442Lys
NM_000036.2:c.1324G>A	NP_000027.2:p.Glu442Lys
NM_001172626.1:c.1312G>A	NP_001166097.1:p.Glu438Lys
NM_000036.3:c.1225G>A MANE Select	NP_000027.3:p.Glu409Lys
NM_001172626.2:c.1213G>A	NP_001166097.2:p.Glu405Lys