Canonical Allele Identifier: CA1190276363
Gene: AMPD1 HGNC NCBI

Linked Data

dbSNP Id: rs1658027612

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677619del , CM000663.2:g.114677619del GRCh38
NC_000001.10:g.115220240del , CM000663.1:g.115220240del GRCh37
NC_000001.9:g.115021763del NCBI36
NG_008012.1:g.22940del

Transcript Alleles

HGVS Amino-acid change
ENST00000369538.4:c.1213-102del ENSP00000358551.4:n.1213-102del
ENST00000520113.7:c.1225-102del MANE Select ENSP00000430075.3:n.1225-102del
ENST00000637080.1:c.1008-102del ENSP00000489753.1:n.1008-102del
ENST00000639077.1:n.890-102del
ENST00000369538.3:c.1312-102del ENSP00000358551.3:n.1312-102del
ENST00000520113.6:c.1324-102del ENSP00000430075.2:n.1324-102del
NM_000036.2:c.1324-102del NP_000027.2:n.1324-102del
NM_001172626.1:c.1312-102del NP_001166097.1:n.1312-102del
NM_000036.3:c.1225-102del MANE Select NP_000027.3:n.1225-102del
NM_001172626.2:c.1213-102del NP_001166097.2:n.1213-102del