Canonical Allele Identifier: CA2647247410

Gene: AMPD1

Linked Data

• gnomAD v4: 1-114677759-TCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677760_114677762del , CM000663.2:g.114677760_114677762del	GRCh38
NC_000001.10:g.115220381_115220383del , CM000663.1:g.115220381_115220383del	GRCh37
NC_000001.9:g.115021904_115021906del	NCBI36
NG_008012.1:g.22794_22796del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369538.4:c.1212+148_1212+150del	ENSP00000358551.4:n.1212+148_1212+150del
ENST00000520113.7:c.1224+148_1224+150del MANE Select	ENSP00000430075.3:n.1224+148_1224+150del
ENST00000637080.1:c.1007+148_1007+150del	ENSP00000489753.1:n.1007+148_1007+150del
ENST00000639077.1:n.889+148_889+150del
ENST00000369538.3:c.1311+148_1311+150del	ENSP00000358551.3:n.1311+148_1311+150del
ENST00000520113.6:c.1323+148_1323+150del	ENSP00000430075.2:n.1323+148_1323+150del
NM_000036.2:c.1323+148_1323+150del	NP_000027.2:n.1323+148_1323+150del
NM_001172626.1:c.1311+148_1311+150del	NP_001166097.1:n.1311+148_1311+150del
NM_000036.3:c.1224+148_1224+150del MANE Select	NP_000027.3:n.1224+148_1224+150del
NM_001172626.2:c.1212+148_1212+150del	NP_001166097.2:n.1212+148_1212+150del