Canonical Allele Identifier: CA2667574790

Gene: GP9

Linked Data

• gnomAD v4: 3-129061869-A-ACGGCCCTGC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061871_129061879dup , CM000665.2:g.129061871_129061879dup	GRCh38
NC_000003.11:g.128780714_128780722dup , CM000665.1:g.128780714_128780722dup	GRCh37
NC_000003.10:g.130263404_130263412dup	NCBI36
NG_008715.1:g.6070_6078dup , LRG_477:g.6070_6078dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.132_140dup MANE Select	ENSP00000303942.4:p.Pro47_Ala48insAlaLeuPro
ENST00000307395.4:c.132_140dup	ENSP00000303942.4:p.Pro47_Ala48insAlaLeuPro
NM_000174.4:c.132_140dup , LRG_477t1:c.132_140dup	NP_000165.1:p.Pro47_Ala48insAlaLeuPro
XM_005247374.3:c.132_140dup	XP_005247431.1:p.Pro47_Ala48insAlaLeuPro
XM_011512701.1:c.132_140dup	XP_011511003.1:p.Pro47_Ala48insAlaLeuPro
XM_011512702.1:c.132_140dup	XP_011511004.1:p.Pro47_Ala48insAlaLeuPro
NM_000174.5:c.132_140dup MANE Select	NP_000165.1:p.Pro47_Ala48insAlaLeuPro