Canonical Allele Identifier: CA898688375

Gene: GP9

Linked Data

• dbSNP Id: rs1414734282
• MyVariant Identifiers: chr3:g.128780346_128780349del (hg19) ; chr3:g.129061503_129061506del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061506_129061509del , CM000665.2:g.129061506_129061509del	GRCh38
NC_000003.11:g.128780349_128780352del , CM000665.1:g.128780349_128780352del	GRCh37
NC_000003.10:g.130263039_130263042del	NCBI36
NG_008715.1:g.5705_5708del , LRG_477:g.5705_5708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-126_-123del MANE Select	ENSP00000303942.4:n.-126_-123del
ENST00000307395.4:c.-126_-123del	ENSP00000303942.4:n.-126_-123del
NM_000174.4:c.-126_-123del , LRG_477t1:c.-126_-123del	NP_000165.1:n.-126_-123del
XM_005247374.3:c.-126_-123del	XP_005247431.1:n.-126_-123del
XM_011512701.1:c.-126_-123del	XP_011511003.1:n.-126_-123del
XM_011512702.1:c.-12-222_-12-219del	XP_011511004.1:n.-12-222_-12-219del
NM_000174.5:c.-126_-123del MANE Select	NP_000165.1:n.-126_-123del