Canonical Allele Identifier: CA3039273442
Gene: AMPD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114677799_114677807delinsCTCCTTCCT , CM000663.2:g.114677799_114677807delinsCTCCTTCCT GRCh38
NC_000001.10:g.115220420_115220428delinsCTCCTTCCT , CM000663.1:g.115220420_115220428delinsCTCCTTCCT GRCh37
NC_000001.9:g.115021943_115021951delinsCTCCTTCCT NCBI36
NG_008012.1:g.22749_22757delinsAGGAAGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369538.4:c.1212+103_1212+111delinsAGGAAGGAG ENSP00000358551.4:n.1212+103_1212+111delinsAGGAAGGAG
ENST00000520113.7:c.1224+103_1224+111delinsAGGAAGGAG MANE Select ENSP00000430075.3:n.1224+103_1224+111delinsAGGAAGGAG
ENST00000637080.1:c.1007+103_1007+111delinsAGGAAGGAG ENSP00000489753.1:n.1007+103_1007+111delinsAGGAAGGAG
ENST00000639077.1:n.889+103_889+111delinsAGGAAGGAG
ENST00000369538.3:c.1311+103_1311+111delinsAGGAAGGAG ENSP00000358551.3:n.1311+103_1311+111delinsAGGAAGGAG
ENST00000520113.6:c.1323+103_1323+111delinsAGGAAGGAG ENSP00000430075.2:n.1323+103_1323+111delinsAGGAAGGAG
NM_000036.2:c.1323+103_1323+111delinsAGGAAGGAG NP_000027.2:n.1323+103_1323+111delinsAGGAAGGAG
NM_001172626.1:c.1311+103_1311+111delinsAGGAAGGAG NP_001166097.1:n.1311+103_1311+111delinsAGGAAGGAG
NM_000036.3:c.1224+103_1224+111delinsAGGAAGGAG MANE Select NP_000027.3:n.1224+103_1224+111delinsAGGAAGGAG
NM_001172626.2:c.1212+103_1212+111delinsAGGAAGGAG NP_001166097.2:n.1212+103_1212+111delinsAGGAAGGAG