Canonical Allele Identifier: CA341752649

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226914C>T (hg19) ; chr1:g.114684293C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684293C>T , CM000663.2:g.114684293C>T	GRCh38
NC_000001.10:g.115226914C>T , CM000663.1:g.115226914C>T	GRCh37
NC_000001.9:g.115028437C>T	NCBI36
NG_008012.1:g.16263G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.441G>A	ENSP00000358551.4:p.Met147Ile
ENST00000520113.7:c.453G>A MANE Select	ENSP00000430075.3:p.Met151Ile
ENST00000637080.1:c.456G>A	ENSP00000489753.1:p.Met152Ile
ENST00000639077.1:n.118G>A
ENST00000369538.3:c.540G>A	ENSP00000358551.3:p.Met180Ile
ENST00000485564.3:n.327G>A
ENST00000520113.6:c.552G>A	ENSP00000430075.2:p.Met184Ile
NM_000036.2:c.552G>A	NP_000027.2:p.Met184Ile
NM_001172626.1:c.540G>A	NP_001166097.1:p.Met180Ile
NM_000036.3:c.453G>A MANE Select	NP_000027.3:p.Met151Ile
NM_001172626.2:c.441G>A	NP_001166097.2:p.Met147Ile