Canonical Allele Identifier: CA1401004574

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061628_129061629delinsAC , CM000665.2:g.129061628_129061629delinsAC	GRCh38
NC_000003.11:g.128780471_128780472delinsAC , CM000665.1:g.128780471_128780472delinsAC	GRCh37
NC_000003.10:g.130263161_130263162delinsAC	NCBI36
NG_008715.1:g.5827_5828delinsAC , LRG_477:g.5827_5828delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-13+9_-13+10delinsAC MANE Select	ENSP00000303942.4:n.-13+9_-13+10delinsAC
ENST00000307395.4:c.-13+9_-13+10delinsAC	ENSP00000303942.4:n.-13+9_-13+10delinsAC
NM_000174.4:c.-13+9_-13+10delinsAC , LRG_477t1:c.-13+9_-13+10delinsAC	NP_000165.1:n.-13+9_-13+10delinsAC
XM_005247374.3:c.-13+9_-13+10delinsAC	XP_005247431.1:n.-13+9_-13+10delinsAC
XM_011512701.1:c.-13+9_-13+10delinsAC	XP_011511003.1:n.-13+9_-13+10delinsAC
XM_011512702.1:c.-12-100_-12-99delinsAC	XP_011511004.1:n.-12-100_-12-99delinsAC
NM_000174.5:c.-13+9_-13+10delinsAC MANE Select	NP_000165.1:n.-13+9_-13+10delinsAC