Canonical Allele Identifier: CA221653770

Gene: F2

Linked Data

• dbSNP Id: rs909904487
• gnomAD v2: 11-46749423-ATCTGGGCCCCG-A
• gnomAD v3: 11-46727873-ATCTGGGCCCCG-A
• gnomAD v4: 11-46727873-ATCTGGGCCCCG-A
• MyVariant Identifiers: chr11:g.46749424_46749434del (hg19) ; chr11:g.46727874_46727884del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46727874_46727884del , CM000673.2:g.46727874_46727884del	GRCh38
NC_000011.9:g.46749424_46749434del , CM000673.1:g.46749424_46749434del	GRCh37
NC_000011.8:g.46706000_46706010del	NCBI36
NG_008953.1:g.13682_13692del , LRG_551:g.13682_13692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.1131-122_1131-112del MANE Select	ENSP00000308541.5:n.1131-122_1131-112del
ENST00000311907.9:c.1131-122_1131-112del	ENSP00000308541.5:n.1131-122_1131-112del
ENST00000530231.5:c.1131-122_1131-112del	ENSP00000433907.1:n.1131-122_1131-112del
NM_000506.3:c.1131-122_1131-112del	NP_000497.1:n.1131-122_1131-112del
NM_000506.4:c.1131-122_1131-112del , LRG_551t1:c.1131-122_1131-112del	NP_000497.1:n.1131-122_1131-112del
NM_001311257.1:c.1083-122_1083-112del	NP_001298186.1:n.1083-122_1083-112del
XR_428840.2:n.1175-122_1175-112del
XR_428840.4:n.1166-122_1166-112del
NM_000506.5:c.1131-122_1131-112del MANE Select	NP_000497.1:n.1131-122_1131-112del
NM_001311257.2:c.1083-122_1083-112del	NP_001298186.1:n.1083-122_1083-112del