Canonical Allele Identifier: CA2647253059

Gene: AMPD1

Linked Data

• gnomAD v4: 1-114684106-C-CTGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684108_114684111dup , CM000663.2:g.114684108_114684111dup	GRCh38
NC_000001.10:g.115226729_115226732dup , CM000663.1:g.115226729_115226732dup	GRCh37
NC_000001.9:g.115028252_115028255dup	NCBI36
NG_008012.1:g.16446_16449dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.535+89_535+92dup	ENSP00000358551.4:n.535+89_535+92dup
ENST00000520113.7:c.547+89_547+92dup MANE Select	ENSP00000430075.3:n.547+89_547+92dup
ENST00000637080.1:c.550+89_550+92dup	ENSP00000489753.1:n.550+89_550+92dup
ENST00000639077.1:n.212+89_212+92dup
ENST00000369538.3:c.634+89_634+92dup	ENSP00000358551.3:n.634+89_634+92dup
ENST00000485564.3:n.421+89_421+92dup
ENST00000520113.6:c.646+89_646+92dup	ENSP00000430075.2:n.646+89_646+92dup
NM_000036.2:c.646+89_646+92dup	NP_000027.2:n.646+89_646+92dup
NM_001172626.1:c.634+89_634+92dup	NP_001166097.1:n.634+89_634+92dup
NM_000036.3:c.547+89_547+92dup MANE Select	NP_000027.3:n.547+89_547+92dup
NM_001172626.2:c.535+89_535+92dup	NP_001166097.2:n.535+89_535+92dup