Canonical Allele Identifier: CA546191208

Gene: GP9

Linked Data

• dbSNP Id: rs1418907902
• gnomAD v2: 3-128780433-AGAG-A
• gnomAD v3: 3-129061590-AGAG-A
• gnomAD v4: 3-129061590-AGAG-A
• MyVariant Identifiers: chr3:g.128780434_128780436del (hg19) ; chr3:g.129061591_129061593del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061594_129061596del , CM000665.2:g.129061594_129061596del	GRCh38
NC_000003.11:g.128780437_128780439del , CM000665.1:g.128780437_128780439del	GRCh37
NC_000003.10:g.130263127_130263129del	NCBI36
NG_008715.1:g.5793_5795del , LRG_477:g.5793_5795del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-38_-36del MANE Select	ENSP00000303942.4:n.-38_-36del
ENST00000307395.4:c.-38_-36del	ENSP00000303942.4:n.-38_-36del
NM_000174.4:c.-38_-36del , LRG_477t1:c.-38_-36del	NP_000165.1:n.-38_-36del
XM_005247374.3:c.-38_-36del	XP_005247431.1:n.-38_-36del
XM_011512701.1:c.-38_-36del	XP_011511003.1:n.-38_-36del
XM_011512702.1:c.-12-134_-12-132del	XP_011511004.1:n.-12-134_-12-132del
NM_000174.5:c.-38_-36del MANE Select	NP_000165.1:n.-38_-36del