Canonical Allele Identifier: CA341748717

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220110G>A (hg19) ; chr1:g.114677489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677489G>A , CM000663.2:g.114677489G>A	GRCh38
NC_000001.10:g.115220110G>A , CM000663.1:g.115220110G>A	GRCh37
NC_000001.9:g.115021633G>A	NCBI36
NG_008012.1:g.23067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1238C>T	ENSP00000358551.4:p.Ala413Val
ENST00000520113.7:c.1250C>T MANE Select	ENSP00000430075.3:p.Ala417Val
ENST00000637080.1:c.1033C>T	ENSP00000489753.1:n.1033C>T
ENST00000639077.1:n.915C>T
ENST00000369538.3:c.1337C>T	ENSP00000358551.3:p.Ala446Val
ENST00000520113.6:c.1349C>T	ENSP00000430075.2:p.Ala450Val
NM_000036.2:c.1349C>T	NP_000027.2:p.Ala450Val
NM_001172626.1:c.1337C>T	NP_001166097.1:p.Ala446Val
NM_000036.3:c.1250C>T MANE Select	NP_000027.3:p.Ala417Val
NM_001172626.2:c.1238C>T	NP_001166097.2:p.Ala413Val