Canonical Allele Identifier: CA2758355601

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061866_129061867insACAACCAACCAAACACACCCA , CM000665.2:g.129061866_129061867insACAACCAACCAAACACACCCA	GRCh38
NC_000003.11:g.128780709_128780710insACAACCAACCAAACACACCCA , CM000665.1:g.128780709_128780710insACAACCAACCAAACACACCCA	GRCh37
NC_000003.10:g.130263399_130263400insACAACCAACCAAACACACCCA	NCBI36
NG_008715.1:g.6065_6066insACAACCAACCAAACACACCCA , LRG_477:g.6065_6066insACAACCAACCAAACACACCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.127_128insACAACCAACCAAACACACCCA MANE Select	ENSP00000303942.4:p.Leu43delinsHisAsnGlnProAsnThrProIle
ENST00000307395.4:c.127_128insACAACCAACCAAACACACCCA	ENSP00000303942.4:p.Leu43delinsHisAsnGlnProAsnThrProIle
NM_000174.4:c.127_128insACAACCAACCAAACACACCCA , LRG_477t1:c.127_128insACAACCAACCAAACACACCCA	NP_000165.1:p.Leu43delinsHisAsnGlnProAsnThrProIle
XM_005247374.3:c.127_128insACAACCAACCAAACACACCCA	XP_005247431.1:p.Leu43delinsHisAsnGlnProAsnThrProIle
XM_011512701.1:c.127_128insACAACCAACCAAACACACCCA	XP_011511003.1:p.Leu43delinsHisAsnGlnProAsnThrProIle
XM_011512702.1:c.127_128insACAACCAACCAAACACACCCA	XP_011511004.1:p.Leu43delinsHisAsnGlnProAsnThrProIle
NM_000174.5:c.127_128insACAACCAACCAAACACACCCA MANE Select	NP_000165.1:p.Leu43delinsHisAsnGlnProAsnThrProIle