Canonical Allele Identifier: CA341749125

Gene: AMPD1

Linked Data

• MyVariant Identifiers: chr1:g.115220616T>G (hg19) ; chr1:g.114677995T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677995T>G , CM000663.2:g.114677995T>G	GRCh38
NC_000001.10:g.115220616T>G , CM000663.1:g.115220616T>G	GRCh37
NC_000001.9:g.115022139T>G	NCBI36
NG_008012.1:g.22561A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1127A>C	ENSP00000358551.4:p.Asn376Thr
ENST00000520113.7:c.1139A>C MANE Select	ENSP00000430075.3:p.Asn380Thr
ENST00000637080.1:c.922A>C	ENSP00000489753.1:n.922A>C
ENST00000639077.1:n.804A>C
ENST00000369538.3:c.1226A>C	ENSP00000358551.3:p.Asn409Thr
ENST00000520113.6:c.1238A>C	ENSP00000430075.2:p.Asn413Thr
NM_000036.2:c.1238A>C	NP_000027.2:p.Asn413Thr
NM_001172626.1:c.1226A>C	NP_001166097.1:p.Asn409Thr
NM_000036.3:c.1139A>C MANE Select	NP_000027.3:p.Asn380Thr
NM_001172626.2:c.1127A>C	NP_001166097.2:p.Asn376Thr