Canonical Allele Identifier: CA2623803939

Gene: F7

Linked Data

• gnomAD v4: 13-113114071-G-GGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114071_113114072insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA , CM000675.2:g.113114071_113114072insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	GRCh38
NC_000013.10:g.113768385_113768386insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA , CM000675.1:g.113768385_113768386insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	GRCh37
NC_000013.9:g.112816386_112816387insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	NCBI36
NG_009262.1:g.13281_13282insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA , LRG_554:g.13281_13282insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA MANE Select	ENSP00000329546.4:n.364+111_364+112insGTGGTGATCATCCACTCACCACT...
ENST00000346342.7:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	ENSP00000329546.3:n.364+111_364+112insGTGGTGATCATCCACTCACCACT...
ENST00000375581.3:c.430+111_430+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	ENSP00000364731.3:n.430+111_430+112insGTGGTGATCATCCACTCACCACT...
ENST00000444337.1:c.*172+111_*172+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	ENSP00000387669.1:n.*172+111_*172+112insGTGGTGATCATCCACTCACCA...
ENST00000473085.1:n.311+111_311+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA
ENST00000479674.1:n.697+111_697+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA
ENST00000541084.5:c.178+111_178+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	ENSP00000442051.2:n.178+111_178+112insGTGGTGATCATCCACTCACCACT...
NM_000131.4:c.430+111_430+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA , LRG_554t1:c.430+111_430+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	NP_000122.1:n.430+111_430+112insGTGGTGATCATCCACTCACCACTGTAAGA...
NM_001267554.1:c.178+111_178+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	NP_001254483.1:n.178+111_178+112insGTGGTGATCATCCACTCACCACTGTA...
NM_019616.3:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA , LRG_554t2:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	NP_062562.1:n.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGA...
NR_051961.1:n.451+111_451+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA
XM_006719963.2:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_006720026.1:n.364+111_364+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537474.1:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535776.1:n.364+111_364+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537475.1:c.178+111_178+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535777.1:n.178+111_178+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537477.1:c.325+111_325+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535779.1:n.325+111_325+112insGTGGTGATCATCCACTCACCACTGTA...
XM_006719963.3:c.409+111_409+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_006720026.2:n.409+111_409+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537474.2:c.409+111_409+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535776.2:n.409+111_409+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537475.2:c.223+111_223+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535777.2:n.223+111_223+112insGTGGTGATCATCCACTCACCACTGTA...
XM_011537476.2:c.-698_-697insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	XP_011535778.1:n.-698_-697insGTGGTGATCATCCACTCACCACTGTAAGAAAT...
NM_019616.4:c.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA MANE Select	NP_062562.1:n.364+111_364+112insGTGGTGATCATCCACTCACCACTGTAAGA...
NR_051961.2:n.448+111_448+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA
NM_001267554.2:c.178+111_178+112insGTGGTGATCATCCACTCACCACTGTAAGAAATCCAGAA	NP_001254483.1:n.178+111_178+112insGTGGTGATCATCCACTCACCACTGTA...