Canonical Allele Identifier: CA1005999492

Gene: AMPD1

Linked Data

• dbSNP Id: rs1557969503
• gnomAD v3: 1-114677799-C-CCTTCCTTCCT
• gnomAD v4: 1-114677799-C-CCTTCCTTCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114677799_114677800insCTTCCTTCCT , CM000663.2:g.114677799_114677800insCTTCCTTCCT	GRCh38
NC_000001.10:g.115220420_115220421insCTTCCTTCCT , CM000663.1:g.115220420_115220421insCTTCCTTCCT	GRCh37
NC_000001.9:g.115021943_115021944insCTTCCTTCCT	NCBI36
NG_008012.1:g.22756_22757insAGGAAGGAAG

Transcript Alleles

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