Canonical Allele Identifier: CA2703971117

Gene: GP9

Linked Data

• dbSNP Id: rs2107956376

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061783del , CM000665.2:g.129061783del	GRCh38
NC_000003.11:g.128780626del , CM000665.1:g.128780626del	GRCh37
NC_000003.10:g.130263316del	NCBI36
NG_008715.1:g.5982del , LRG_477:g.5982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.44del MANE Select	ENSP00000303942.4:p.Glu15GlyfsTer?
ENST00000307395.4:c.44del	ENSP00000303942.4:p.Glu15GlyfsTer?
NM_000174.4:c.44del , LRG_477t1:c.44del	NP_000165.1:p.Glu15GlyfsTer?
XM_005247374.3:c.44del	XP_005247431.1:p.Glu15GlyfsTer?
XM_011512701.1:c.44del	XP_011511003.1:p.Glu15GlyfsTer?
XM_011512702.1:c.44del	XP_011511004.1:p.Glu15GlyfsTer?
NM_000174.5:c.44del MANE Select	NP_000165.1:p.Glu15GlyfsTer?