Canonical Allele Identifier: CA341752547

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115226886T>C (hg19) ; chr1:g.114684265T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684265T>C , CM000663.2:g.114684265T>C	GRCh38
NC_000001.10:g.115226886T>C , CM000663.1:g.115226886T>C	GRCh37
NC_000001.9:g.115028409T>C	NCBI36
NG_008012.1:g.16291A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.469A>G	ENSP00000358551.4:p.Thr157Ala
ENST00000520113.7:c.481A>G MANE Select	ENSP00000430075.3:p.Thr161Ala
ENST00000637080.1:c.484A>G	ENSP00000489753.1:p.Thr162Ala
ENST00000639077.1:n.146A>G
ENST00000369538.3:c.568A>G	ENSP00000358551.3:p.Thr190Ala
ENST00000485564.3:n.355A>G
ENST00000520113.6:c.580A>G	ENSP00000430075.2:p.Thr194Ala
NM_000036.2:c.580A>G	NP_000027.2:p.Thr194Ala
NM_001172626.1:c.568A>G	NP_001166097.1:p.Thr190Ala
NM_000036.3:c.481A>G MANE Select	NP_000027.3:p.Thr161Ala
NM_001172626.2:c.469A>G	NP_001166097.2:p.Thr157Ala