Canonical Allele Identifier: CA2120144664

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119750_113119752delinsCAG , CM000675.2:g.113119750_113119752delinsCAG	GRCh38
NC_000013.10:g.113774064_113774066delinsCAG , CM000675.1:g.113774064_113774066delinsCAG	GRCh37
NC_000013.9:g.112822065_112822067delinsCAG	NCBI36
NG_009258.1:g.1952_1954delinsCAG , LRG_548:g.1952_1954delinsCAG
NG_009262.1:g.18960_18962delinsCAG , LRG_554:g.18960_18962delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*742_*744delinsCAG MANE Select	ENSP00000329546.4:n.*742_*744delinsCAG
ENST00000346342.7:c.*742_*744delinsCAG	ENSP00000329546.3:n.*742_*744delinsCAG
ENST00000375581.3:c.*742_*744delinsCAG	ENSP00000364731.3:n.*742_*744delinsCAG
ENST00000541084.5:c.*742_*744delinsCAG	ENSP00000442051.2:n.*742_*744delinsCAG
NM_000131.4:c.*742_*744delinsCAG , LRG_554t1:c.*742_*744delinsCAG	NP_000122.1:n.*742_*744delinsCAG
NM_001267554.1:c.*742_*744delinsCAG	NP_001254483.1:n.*742_*744delinsCAG
NM_019616.3:c.*742_*744delinsCAG , LRG_554t2:c.*742_*744delinsCAG	NP_062562.1:n.*742_*744delinsCAG
NR_051961.1:n.2164_2166delinsCAG
XM_006719963.2:c.*742_*744delinsCAG	XP_006720026.1:n.*742_*744delinsCAG
XM_011537474.1:c.*742_*744delinsCAG	XP_011535776.1:n.*742_*744delinsCAG
XM_011537475.1:c.*742_*744delinsCAG	XP_011535777.1:n.*742_*744delinsCAG
XM_011537476.1:c.*742_*744delinsCAG	XP_011535778.1:n.*742_*744delinsCAG
XM_011537477.1:c.*742_*744delinsCAG	XP_011535779.1:n.*742_*744delinsCAG
XM_006719963.3:c.*742_*744delinsCAG	XP_006720026.2:n.*742_*744delinsCAG
XM_011537474.2:c.*742_*744delinsCAG	XP_011535776.2:n.*742_*744delinsCAG
XM_011537475.2:c.*742_*744delinsCAG	XP_011535777.2:n.*742_*744delinsCAG
XM_011537476.2:c.*742_*744delinsCAG	XP_011535778.1:n.*742_*744delinsCAG
NM_019616.4:c.*742_*744delinsCAG MANE Select	NP_062562.1:n.*742_*744delinsCAG
NR_051961.2:n.2161_2163delinsCAG
NM_001267554.2:c.*742_*744delinsCAG	NP_001254483.1:n.*742_*744delinsCAG