Canonical Allele Identifier: CA2667574702

Gene: GP9

Linked Data

• gnomAD v4: 3-129061652-T-TAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061654_129061655dup , CM000665.2:g.129061654_129061655dup	GRCh38
NC_000003.11:g.128780497_128780498dup , CM000665.1:g.128780497_128780498dup	GRCh37
NC_000003.10:g.130263187_130263188dup	NCBI36
NG_008715.1:g.5853_5854dup , LRG_477:g.5853_5854dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000307395.5:c.-13+35_-13+36dup MANE Select	ENSP00000303942.4:n.-13+35_-13+36dup
ENST00000307395.4:c.-13+35_-13+36dup	ENSP00000303942.4:n.-13+35_-13+36dup
NM_000174.4:c.-13+35_-13+36dup , LRG_477t1:c.-13+35_-13+36dup	NP_000165.1:n.-13+35_-13+36dup
XM_005247374.3:c.-13+35_-13+36dup	XP_005247431.1:n.-13+35_-13+36dup
XM_011512701.1:c.-13+35_-13+36dup	XP_011511003.1:n.-13+35_-13+36dup
XM_011512702.1:c.-12-74_-12-73dup	XP_011511004.1:n.-12-74_-12-73dup
NM_000174.5:c.-13+35_-13+36dup MANE Select	NP_000165.1:n.-13+35_-13+36dup