Canonical Allele Identifier: CA1190281664

Gene: AMPD1

Linked Data

• dbSNP Id: rs1658240655

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114684152del , CM000663.2:g.114684152del	GRCh38
NC_000001.10:g.115226773del , CM000663.1:g.115226773del	GRCh37
NC_000001.9:g.115028296del	NCBI36
NG_008012.1:g.16404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.535+47del	ENSP00000358551.4:n.535+47del
ENST00000520113.7:c.547+47del MANE Select	ENSP00000430075.3:n.547+47del
ENST00000637080.1:c.550+47del	ENSP00000489753.1:n.550+47del
ENST00000639077.1:n.212+47del
ENST00000369538.3:c.634+47del	ENSP00000358551.3:n.634+47del
ENST00000485564.3:n.421+47del
ENST00000520113.6:c.646+47del	ENSP00000430075.2:n.646+47del
NM_000036.2:c.646+47del	NP_000027.2:n.646+47del
NM_001172626.1:c.634+47del	NP_001166097.1:n.634+47del
NM_000036.3:c.547+47del MANE Select	NP_000027.3:n.547+47del
NM_001172626.2:c.535+47del	NP_001166097.2:n.535+47del