Canonical Allele Identifier: CA341752671

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226919A>T (hg19) ; chr1:g.114684298A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684298A>T , CM000663.2:g.114684298A>T	GRCh38
NC_000001.10:g.115226919A>T , CM000663.1:g.115226919A>T	GRCh37
NC_000001.9:g.115028442A>T	NCBI36
NG_008012.1:g.16258T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.436T>A	ENSP00000358551.4:p.Tyr146Asn
ENST00000520113.7:c.448T>A MANE Select	ENSP00000430075.3:p.Tyr150Asn
ENST00000637080.1:c.451T>A	ENSP00000489753.1:p.Tyr151Asn
ENST00000639077.1:n.113T>A
ENST00000369538.3:c.535T>A	ENSP00000358551.3:p.Tyr179Asn
ENST00000485564.3:n.322T>A
ENST00000520113.6:c.547T>A	ENSP00000430075.2:p.Tyr183Asn
NM_000036.2:c.547T>A	NP_000027.2:p.Tyr183Asn
NM_001172626.1:c.535T>A	NP_001166097.1:p.Tyr179Asn
NM_000036.3:c.448T>A MANE Select	NP_000027.3:p.Tyr150Asn
NM_001172626.2:c.436T>A	NP_001166097.2:p.Tyr146Asn