Canonical Allele Identifier: CA2667574512

Gene: GP9

Linked Data

• gnomAD v4: 3-129061434-CTCTGCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061435_129061440del , CM000665.2:g.129061435_129061440del	GRCh38
NC_000003.11:g.128780278_128780283del , CM000665.1:g.128780278_128780283del	GRCh37
NC_000003.10:g.130262968_130262973del	NCBI36
NG_008715.1:g.5634_5639del , LRG_477:g.5634_5639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-138-59_-138-54del MANE Select	ENSP00000303942.4:n.-138-59_-138-54del
ENST00000307395.4:c.-138-59_-138-54del	ENSP00000303942.4:n.-138-59_-138-54del
NM_000174.4:c.-138-59_-138-54del , LRG_477t1:c.-138-59_-138-54del	NP_000165.1:n.-138-59_-138-54del
XM_005247374.3:c.-138-59_-138-54del	XP_005247431.1:n.-138-59_-138-54del
XM_011512701.1:c.-138-59_-138-54del	XP_011511003.1:n.-138-59_-138-54del
XM_011512702.1:c.-12-293_-12-288del	XP_011511004.1:n.-12-293_-12-288del
NM_000174.5:c.-138-59_-138-54del MANE Select	NP_000165.1:n.-138-59_-138-54del