Canonical Allele Identifier: CA1401004504

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061502_129061506delinsACCGC , CM000665.2:g.129061502_129061506delinsACCGC	GRCh38
NC_000003.11:g.128780345_128780349delinsACCGC , CM000665.1:g.128780345_128780349delinsACCGC	GRCh37
NC_000003.10:g.130263035_130263039delinsACCGC	NCBI36
NG_008715.1:g.5701_5705delinsACCGC , LRG_477:g.5701_5705delinsACCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-130_-126delinsACCGC MANE Select	ENSP00000303942.4:n.-130_-126delinsACCGC
ENST00000307395.4:c.-130_-126delinsACCGC	ENSP00000303942.4:n.-130_-126delinsACCGC
NM_000174.4:c.-130_-126delinsACCGC , LRG_477t1:c.-130_-126delinsACCGC	NP_000165.1:n.-130_-126delinsACCGC
XM_005247374.3:c.-130_-126delinsACCGC	XP_005247431.1:n.-130_-126delinsACCGC
XM_011512701.1:c.-130_-126delinsACCGC	XP_011511003.1:n.-130_-126delinsACCGC
XM_011512702.1:c.-12-226_-12-222delinsACCGC	XP_011511004.1:n.-12-226_-12-222delinsACCGC
NM_000174.5:c.-130_-126delinsACCGC MANE Select	NP_000165.1:n.-130_-126delinsACCGC