Canonical Allele Identifier: CA2647247600

Gene: AMPD1

Linked Data

• gnomAD v4: 1-114677799-C-CTCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677802_114677803insGTCC , CM000663.2:g.114677802_114677803insGTCC	GRCh38
NC_000001.10:g.115220423_115220424insGTCC , CM000663.1:g.115220423_115220424insGTCC	GRCh37
NC_000001.9:g.115021946_115021947insGTCC	NCBI36
NG_008012.1:g.22756_22757insCGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000369538.4:c.1212+110_1212+111insCGGA	ENSP00000358551.4:n.1212+110_1212+111insC...
ENST00000520113.7:c.1224+110_1224+111insCGGA MANE Select	ENSP00000430075.3:n.1224+110_1224+111insC...
ENST00000637080.1:c.1007+110_1007+111insCGGA	ENSP00000489753.1:n.1007+110_1007+111insC...
ENST00000639077.1:n.889+110_889+111insCGGA
ENST00000369538.3:c.1311+110_1311+111insCGGA	ENSP00000358551.3:n.1311+110_1311+111insC...
ENST00000520113.6:c.1323+110_1323+111insCGGA	ENSP00000430075.2:n.1323+110_1323+111insC...
NM_000036.2:c.1323+110_1323+111insCGGA	NP_000027.2:n.1323+110_1323+111insCGGA
NM_001172626.1:c.1311+110_1311+111insCGGA	NP_001166097.1:n.1311+110_1311+111insCGGA...
NM_000036.3:c.1224+110_1224+111insCGGA MANE Select	NP_000027.3:n.1224+110_1224+111insCGGA
NM_001172626.2:c.1212+110_1212+111insCGGA	NP_001166097.2:n.1212+110_1212+111insCGGA...