Canonical Allele Identifier: CA2613335275

Gene: F2

Linked Data

• gnomAD v4: 11-46726523-AGATGGGCTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726528_46726536del , CM000673.2:g.46726528_46726536del	GRCh38
NC_000011.9:g.46748078_46748086del , CM000673.1:g.46748078_46748086del	GRCh37
NC_000011.8:g.46704654_46704662del	NCBI36
NG_008953.1:g.12336_12344del , LRG_551:g.12336_12344del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.905_913del MANE Select	ENSP00000308541.5:p.Gly302_Asp304del
ENST00000311907.9:c.905_913del	ENSP00000308541.5:p.Gly302_Asp304del
ENST00000442468.1:c.875_883del	ENSP00000387413.1:p.Gly292_Asp294del
ENST00000530231.5:c.905_913del	ENSP00000433907.1:p.Gly302_Asp304del
NM_000506.3:c.905_913del	NP_000497.1:p.Gly302_Asp304del
NM_000506.4:c.905_913del , LRG_551t1:c.905_913del	NP_000497.1:p.Gly302_Asp304del
NM_001311257.1:c.857_865del	NP_001298186.1:p.Gly286_Asp288del
XR_428840.2:n.949_957del
XR_428840.4:n.940_948del
NM_000506.5:c.905_913del MANE Select	NP_000497.1:p.Gly302_Asp304del
NM_001311257.2:c.857_865del	NP_001298186.1:p.Gly286_Asp288del