Canonical Allele Identifier: CA2667574492

Gene: GP9

Linked Data

• gnomAD v4: 3-129061412-ATCCCCAAGCAGGGGATGGGGTCTCTGCTAAGGGCCAGGAAGTCCCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061418_129061463del , CM000665.2:g.129061418_129061463del	GRCh38
NC_000003.11:g.128780261_128780306del , CM000665.1:g.128780261_128780306del	GRCh37
NC_000003.10:g.130262951_130262996del	NCBI36
NG_008715.1:g.5617_5662del , LRG_477:g.5617_5662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-138-76_-138-31del MANE Select	ENSP00000303942.4:n.-138-76_-138-31del
ENST00000307395.4:c.-138-76_-138-31del	ENSP00000303942.4:n.-138-76_-138-31del
NM_000174.4:c.-138-76_-138-31del , LRG_477t1:c.-138-76_-138-31del	NP_000165.1:n.-138-76_-138-31del
XM_005247374.3:c.-138-76_-138-31del	XP_005247431.1:n.-138-76_-138-31del
XM_011512701.1:c.-138-76_-138-31del	XP_011511003.1:n.-138-76_-138-31del
XM_011512702.1:c.-12-310_-12-265del	XP_011511004.1:n.-12-310_-12-265del
NM_000174.5:c.-138-76_-138-31del MANE Select	NP_000165.1:n.-138-76_-138-31del