Canonical Allele Identifier: CA341752467

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226865T>A (hg19) ; chr1:g.114684244T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684244T>A , CM000663.2:g.114684244T>A	GRCh38
NC_000001.10:g.115226865T>A , CM000663.1:g.115226865T>A	GRCh37
NC_000001.9:g.115028388T>A	NCBI36
NG_008012.1:g.16312A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.490A>T	ENSP00000358551.4:p.Asn164Tyr
ENST00000520113.7:c.502A>T MANE Select	ENSP00000430075.3:p.Asn168Tyr
ENST00000637080.1:c.505A>T	ENSP00000489753.1:p.Asn169Tyr
ENST00000639077.1:n.167A>T
ENST00000369538.3:c.589A>T	ENSP00000358551.3:p.Asn197Tyr
ENST00000485564.3:n.376A>T
ENST00000520113.6:c.601A>T	ENSP00000430075.2:p.Asn201Tyr
NM_000036.2:c.601A>T	NP_000027.2:p.Asn201Tyr
NM_001172626.1:c.589A>T	NP_001166097.1:p.Asn197Tyr
NM_000036.3:c.502A>T MANE Select	NP_000027.3:p.Asn168Tyr
NM_001172626.2:c.490A>T	NP_001166097.2:p.Asn164Tyr