Canonical Allele Identifier: CA2120135804

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113985_113113986delinsAT , CM000675.2:g.113113985_113113986delinsAT	GRCh38
NC_000013.10:g.113768299_113768300delinsAT , CM000675.1:g.113768299_113768300delinsAT	GRCh37
NC_000013.9:g.112816300_112816301delinsAT	NCBI36
NG_009262.1:g.13195_13196delinsAT , LRG_554:g.13195_13196delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+25_364+26delinsAT MANE Select	ENSP00000329546.4:n.364+25_364+26delinsAT
ENST00000346342.7:c.364+25_364+26delinsAT	ENSP00000329546.3:n.364+25_364+26delinsAT
ENST00000375581.3:c.430+25_430+26delinsAT	ENSP00000364731.3:n.430+25_430+26delinsAT
ENST00000444337.1:c.*172+25_*172+26delinsAT	ENSP00000387669.1:n.*172+25_*172+26delinsAT
ENST00000473085.1:n.311+25_311+26delinsAT
ENST00000479674.1:n.697+25_697+26delinsAT
ENST00000541084.5:c.178+25_178+26delinsAT	ENSP00000442051.2:n.178+25_178+26delinsAT
NM_000131.4:c.430+25_430+26delinsAT , LRG_554t1:c.430+25_430+26delinsAT	NP_000122.1:n.430+25_430+26delinsAT
NM_001267554.1:c.178+25_178+26delinsAT	NP_001254483.1:n.178+25_178+26delinsAT
NM_019616.3:c.364+25_364+26delinsAT , LRG_554t2:c.364+25_364+26delinsAT	NP_062562.1:n.364+25_364+26delinsAT
NR_051961.1:n.451+25_451+26delinsAT
XM_006719963.2:c.364+25_364+26delinsAT	XP_006720026.1:n.364+25_364+26delinsAT
XM_011537474.1:c.364+25_364+26delinsAT	XP_011535776.1:n.364+25_364+26delinsAT
XM_011537475.1:c.178+25_178+26delinsAT	XP_011535777.1:n.178+25_178+26delinsAT
XM_011537477.1:c.325+25_325+26delinsAT	XP_011535779.1:n.325+25_325+26delinsAT
XM_006719963.3:c.409+25_409+26delinsAT	XP_006720026.2:n.409+25_409+26delinsAT
XM_011537474.2:c.409+25_409+26delinsAT	XP_011535776.2:n.409+25_409+26delinsAT
XM_011537475.2:c.223+25_223+26delinsAT	XP_011535777.2:n.223+25_223+26delinsAT
NM_019616.4:c.364+25_364+26delinsAT MANE Select	NP_062562.1:n.364+25_364+26delinsAT
NR_051961.2:n.448+25_448+26delinsAT
NM_001267554.2:c.178+25_178+26delinsAT	NP_001254483.1:n.178+25_178+26delinsAT