Canonical Allele Identifier: CA10639062

Gene: F7

Linked Data

• ClinVar Variation Id: 311250
• ClinVar RCV Id: RCV000353498
• dbSNP Id: rs886049997
• MyVariant Identifiers: chr13:g.113774078_113774092delinsCCA (hg19) ; chr13:g.113119764_113119778delinsCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119764_113119778delinsCCA , CM000675.2:g.113119764_113119778delinsCCA	GRCh38
NC_000013.10:g.113774078_113774092delinsCCA , CM000675.1:g.113774078_113774092delinsCCA	GRCh37
NC_000013.9:g.112822079_112822093delinsCCA	NCBI36
NG_009258.1:g.1966_1980delinsCCA , LRG_548:g.1966_1980delinsCCA
NG_009262.1:g.18974_18988delinsCCA , LRG_554:g.18974_18988delinsCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*756_*770delinsCCA MANE Select	ENSP00000329546.4:n.*756_*770delinsCCA
ENST00000346342.7:c.*756_*770delinsCCA	ENSP00000329546.3:n.*756_*770delinsCCA
ENST00000375581.3:c.*756_*770delinsCCA	ENSP00000364731.3:n.*756_*770delinsCCA
ENST00000541084.5:c.*756_*770delinsCCA	ENSP00000442051.2:n.*756_*770delinsCCA
NM_000131.4:c.*756_*770delinsCCA , LRG_554t1:c.*756_*770delinsCCA	NP_000122.1:n.*756_*770delinsCCA
NM_001267554.1:c.*756_*770delinsCCA	NP_001254483.1:n.*756_*770delinsCCA
NM_019616.3:c.*756_*770delinsCCA , LRG_554t2:c.*756_*770delinsCCA	NP_062562.1:n.*756_*770delinsCCA
NR_051961.1:n.2178_2192delinsCCA
XM_006719963.2:c.*756_*770delinsCCA	XP_006720026.1:n.*756_*770delinsCCA
XM_011537474.1:c.*756_*770delinsCCA	XP_011535776.1:n.*756_*770delinsCCA
XM_011537475.1:c.*756_*770delinsCCA	XP_011535777.1:n.*756_*770delinsCCA
XM_011537476.1:c.*756_*770delinsCCA	XP_011535778.1:n.*756_*770delinsCCA
XM_011537477.1:c.*756_*770delinsCCA	XP_011535779.1:n.*756_*770delinsCCA
XM_006719963.3:c.*756_*770delinsCCA	XP_006720026.2:n.*756_*770delinsCCA
XM_011537474.2:c.*756_*770delinsCCA	XP_011535776.2:n.*756_*770delinsCCA
XM_011537475.2:c.*756_*770delinsCCA	XP_011535777.2:n.*756_*770delinsCCA
XM_011537476.2:c.*756_*770delinsCCA	XP_011535778.1:n.*756_*770delinsCCA
NM_019616.4:c.*756_*770delinsCCA MANE Select	NP_062562.1:n.*756_*770delinsCCA
NR_051961.2:n.2175_2189delinsCCA
NM_001267554.2:c.*756_*770delinsCCA	NP_001254483.1:n.*756_*770delinsCCA