Canonical Allele Identifier: CA2667574784
Gene: GP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061753del , CM000665.2:g.129061753del GRCh38
NC_000003.11:g.128780596del , CM000665.1:g.128780596del GRCh37
NC_000003.10:g.130263286del NCBI36
NG_008715.1:g.5952del , LRG_477:g.5952del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.14del MANE Select ENSP00000303942.4:p.Gly5GlufsTer?
ENST00000307395.4:c.14del ENSP00000303942.4:p.Gly5GlufsTer?
NM_000174.4:c.14del , LRG_477t1:c.14del NP_000165.1:p.Gly5GlufsTer?
XM_005247374.3:c.14del XP_005247431.1:p.Gly5GlufsTer?
XM_011512701.1:c.14del XP_011511003.1:p.Gly5GlufsTer?
XM_011512702.1:c.14del XP_011511004.1:p.Gly5GlufsTer?
NM_000174.5:c.14del MANE Select NP_000165.1:p.Gly5GlufsTer?