Canonical Allele Identifier: CA1190276515

Gene: AMPD1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677817_114677819delinsCCT , CM000663.2:g.114677817_114677819delinsCCT	GRCh38
NC_000001.10:g.115220438_115220440delinsCCT , CM000663.1:g.115220438_115220440delinsCCT	GRCh37
NC_000001.9:g.115021961_115021963delinsCCT	NCBI36
NG_008012.1:g.22737_22739delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1212+91_1212+93delinsAGG	ENSP00000358551.4:n.1212+91_1212+93delinsAGG
ENST00000520113.7:c.1224+91_1224+93delinsAGG MANE Select	ENSP00000430075.3:n.1224+91_1224+93delinsAGG
ENST00000637080.1:c.1007+91_1007+93delinsAGG	ENSP00000489753.1:n.1007+91_1007+93delinsAGG
ENST00000639077.1:n.889+91_889+93delinsAGG
ENST00000369538.3:c.1311+91_1311+93delinsAGG	ENSP00000358551.3:n.1311+91_1311+93delinsAGG
ENST00000520113.6:c.1323+91_1323+93delinsAGG	ENSP00000430075.2:n.1323+91_1323+93delinsAGG
NM_000036.2:c.1323+91_1323+93delinsAGG	NP_000027.2:n.1323+91_1323+93delinsAGG
NM_001172626.1:c.1311+91_1311+93delinsAGG	NP_001166097.1:n.1311+91_1311+93delinsAGG
NM_000036.3:c.1224+91_1224+93delinsAGG MANE Select	NP_000027.3:n.1224+91_1224+93delinsAGG
NM_001172626.2:c.1212+91_1212+93delinsAGG	NP_001166097.2:n.1212+91_1212+93delinsAGG