Canonical Allele Identifier: CA1401004529

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061542_129061543delinsGC , CM000665.2:g.129061542_129061543delinsGC	GRCh38
NC_000003.11:g.128780385_128780386delinsGC , CM000665.1:g.128780385_128780386delinsGC	GRCh37
NC_000003.10:g.130263075_130263076delinsGC	NCBI36
NG_008715.1:g.5741_5742delinsGC , LRG_477:g.5741_5742delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-90_-89delinsGC MANE Select	ENSP00000303942.4:n.-90_-89delinsGC
ENST00000307395.4:c.-90_-89delinsGC	ENSP00000303942.4:n.-90_-89delinsGC
NM_000174.4:c.-90_-89delinsGC , LRG_477t1:c.-90_-89delinsGC	NP_000165.1:n.-90_-89delinsGC
XM_005247374.3:c.-90_-89delinsGC	XP_005247431.1:n.-90_-89delinsGC
XM_011512701.1:c.-90_-89delinsGC	XP_011511003.1:n.-90_-89delinsGC
XM_011512702.1:c.-12-186_-12-185delinsGC	XP_011511004.1:n.-12-186_-12-185delinsGC
NM_000174.5:c.-90_-89delinsGC MANE Select	NP_000165.1:n.-90_-89delinsGC