Canonical Allele Identifier: CA341748460

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220026C>A (hg19) ; chr1:g.114677405C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677405C>A , CM000663.2:g.114677405C>A	GRCh38
NC_000001.10:g.115220026C>A , CM000663.1:g.115220026C>A	GRCh37
NC_000001.9:g.115021549C>A	NCBI36
NG_008012.1:g.23151G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1322G>T	ENSP00000358551.4:p.Cys441Phe
ENST00000520113.7:c.1334G>T MANE Select	ENSP00000430075.3:p.Cys445Phe
ENST00000637080.1:c.1117G>T	ENSP00000489753.1:n.1117G>T
ENST00000639077.1:n.999G>T
ENST00000369538.3:c.1421G>T	ENSP00000358551.3:p.Cys474Phe
ENST00000520113.6:c.1433G>T	ENSP00000430075.2:p.Cys478Phe
NM_000036.2:c.1433G>T	NP_000027.2:p.Cys478Phe
NM_001172626.1:c.1421G>T	NP_001166097.1:p.Cys474Phe
NM_000036.3:c.1334G>T MANE Select	NP_000027.3:p.Cys445Phe
NM_001172626.2:c.1322G>T	NP_001166097.2:p.Cys441Phe