Canonical Allele Identifier: CA341749200

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220646T>G (hg19) ; chr1:g.114678025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114678025T>G , CM000663.2:g.114678025T>G	GRCh38
NC_000001.10:g.115220646T>G , CM000663.1:g.115220646T>G	GRCh37
NC_000001.9:g.115022169T>G	NCBI36
NG_008012.1:g.22531A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1097A>C	ENSP00000358551.4:p.Gln366Pro
ENST00000520113.7:c.1109A>C MANE Select	ENSP00000430075.3:p.Gln370Pro
ENST00000637080.1:c.892A>C	ENSP00000489753.1:n.892A>C
ENST00000639077.1:n.774A>C
ENST00000369538.3:c.1196A>C	ENSP00000358551.3:p.Gln399Pro
ENST00000520113.6:c.1208A>C	ENSP00000430075.2:p.Gln403Pro
NM_000036.2:c.1208A>C	NP_000027.2:p.Gln403Pro
NM_001172626.1:c.1196A>C	NP_001166097.1:p.Gln399Pro
NM_000036.3:c.1109A>C MANE Select	NP_000027.3:p.Gln370Pro
NM_001172626.2:c.1097A>C	NP_001166097.2:p.Gln366Pro