Canonical Allele Identifier: CA2613335551

Gene: F2

Linked Data

• gnomAD v4: 11-46727970-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727971del , CM000673.2:g.46727971del	GRCh38
NC_000011.9:g.46749521del , CM000673.1:g.46749521del	GRCh37
NC_000011.8:g.46706097del	NCBI36
NG_008953.1:g.13779del , LRG_551:g.13779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-25del MANE Select	ENSP00000308541.5:n.1131-25del
ENST00000311907.9:c.1131-25del	ENSP00000308541.5:n.1131-25del
ENST00000530231.5:c.1131-25del	ENSP00000433907.1:n.1131-25del
NM_000506.3:c.1131-25del	NP_000497.1:n.1131-25del
NM_000506.4:c.1131-25del , LRG_551t1:c.1131-25del	NP_000497.1:n.1131-25del
NM_001311257.1:c.1083-25del	NP_001298186.1:n.1083-25del
XR_428840.2:n.1175-25del
XR_428840.4:n.1166-25del
NM_000506.5:c.1131-25del MANE Select	NP_000497.1:n.1131-25del
NM_001311257.2:c.1083-25del	NP_001298186.1:n.1083-25del