Canonical Allele Identifier: CA1969072425

Gene: F2

Linked Data

• dbSNP Id: rs2064872045
• gnomAD v4: 11-46726226-TAAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.46726231_46726233del , CM000673.2:g.46726231_46726233del	GRCh38
NC_000011.9:g.46747781_46747783del , CM000673.1:g.46747781_46747783del	GRCh37
NC_000011.8:g.46704357_46704359del	NCBI36
NG_008953.1:g.12039_12041del , LRG_551:g.12039_12041del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311907.10:c.874+58_874+60del MANE Select	ENSP00000308541.5:n.874+58_874+60del
ENST00000311907.9:c.874+58_874+60del	ENSP00000308541.5:n.874+58_874+60del
ENST00000442468.1:c.844+58_844+60del	ENSP00000387413.1:n.844+58_844+60del
ENST00000530231.5:c.874+58_874+60del	ENSP00000433907.1:n.874+58_874+60del
NM_000506.3:c.874+58_874+60del	NP_000497.1:n.874+58_874+60del
NM_000506.4:c.874+58_874+60del , LRG_551t1:c.874+58_874+60del	NP_000497.1:n.874+58_874+60del
NM_001311257.1:c.826+58_826+60del	NP_001298186.1:n.826+58_826+60del
XR_428840.2:n.918+58_918+60del
XR_428840.4:n.909+58_909+60del
NM_000506.5:c.874+58_874+60del MANE Select	NP_000497.1:n.874+58_874+60del
NM_001311257.2:c.826+58_826+60del	NP_001298186.1:n.826+58_826+60del