Canonical Allele Identifier: CA2667574674

Gene: GP9

Linked Data

• gnomAD v4: 3-129061623-AGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061625_129061626del , CM000665.2:g.129061625_129061626del	GRCh38
NC_000003.11:g.128780468_128780469del , CM000665.1:g.128780468_128780469del	GRCh37
NC_000003.10:g.130263158_130263159del	NCBI36
NG_008715.1:g.5824_5825del , LRG_477:g.5824_5825del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-13+6_-13+7del MANE Select	ENSP00000303942.4:n.-13+6_-13+7del
ENST00000307395.4:c.-13+6_-13+7del	ENSP00000303942.4:n.-13+6_-13+7del
NM_000174.4:c.-13+6_-13+7del , LRG_477t1:c.-13+6_-13+7del	NP_000165.1:n.-13+6_-13+7del
XM_005247374.3:c.-13+6_-13+7del	XP_005247431.1:n.-13+6_-13+7del
XM_011512701.1:c.-13+6_-13+7del	XP_011511003.1:n.-13+6_-13+7del
XM_011512702.1:c.-12-103_-12-102del	XP_011511004.1:n.-12-103_-12-102del
NM_000174.5:c.-13+6_-13+7del MANE Select	NP_000165.1:n.-13+6_-13+7del