Canonical Allele Identifier: CA2667574686

Gene: GP9

Linked Data

• gnomAD v4: 3-129061632-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061632_129061633insAT , CM000665.2:g.129061632_129061633insAT	GRCh38
NC_000003.11:g.128780475_128780476insAT , CM000665.1:g.128780475_128780476insAT	GRCh37
NC_000003.10:g.130263165_130263166insAT	NCBI36
NG_008715.1:g.5831_5832insAT , LRG_477:g.5831_5832insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-13+13_-13+14insAT MANE Select	ENSP00000303942.4:n.-13+13_-13+14insAT
ENST00000307395.4:c.-13+13_-13+14insAT	ENSP00000303942.4:n.-13+13_-13+14insAT
NM_000174.4:c.-13+13_-13+14insAT , LRG_477t1:c.-13+13_-13+14insAT	NP_000165.1:n.-13+13_-13+14insAT
XM_005247374.3:c.-13+13_-13+14insAT	XP_005247431.1:n.-13+13_-13+14insAT
XM_011512701.1:c.-13+13_-13+14insAT	XP_011511003.1:n.-13+13_-13+14insAT
XM_011512702.1:c.-12-96_-12-95insAT	XP_011511004.1:n.-12-96_-12-95insAT
NM_000174.5:c.-13+13_-13+14insAT MANE Select	NP_000165.1:n.-13+13_-13+14insAT