Canonical Allele Identifier: CA2120145042

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119979_113119996delinsGCTTCACAATAAACGGCT , CM000675.2:g.113119979_113119996delinsGCTTCACAATAAACGGCT	GRCh38
NC_000013.10:g.113774293_113774310delinsGCTTCACAATAAACGGCT , CM000675.1:g.113774293_113774310delinsGCTTCACAATAAACGGCT	GRCh37
NC_000013.9:g.112822294_112822311delinsGCTTCACAATAAACGGCT	NCBI36
NG_009258.1:g.2181_2198delinsGCTTCACAATAAACGGCT , LRG_548:g.2181_2198delinsGCTTCACAATAAACGGCT
NG_009262.1:g.19189_19206delinsGCTTCACAATAAACGGCT , LRG_554:g.19189_19206delinsGCTTCACAATAAACGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*971_*988delinsGCTTCACAATAAACGGCT MANE Select	ENSP00000329546.4:n.*971_*988delinsGCTTCACAATAAACGGCT
ENST00000346342.7:c.*971_*988delinsGCTTCACAATAAACGGCT	ENSP00000329546.3:n.*971_*988delinsGCTTCACAATAAACGGCT
ENST00000375581.3:c.*971_*988delinsGCTTCACAATAAACGGCT	ENSP00000364731.3:n.*971_*988delinsGCTTCACAATAAACGGCT
ENST00000541084.5:c.*971_*988delinsGCTTCACAATAAACGGCT	ENSP00000442051.2:n.*971_*988delinsGCTTCACAATAAACGGCT
NM_000131.4:c.*971_*988delinsGCTTCACAATAAACGGCT , LRG_554t1:c.*971_*988delinsGCTTCACAATAAACGGCT	NP_000122.1:n.*971_*988delinsGCTTCACAATAAACGGCT
NM_001267554.1:c.*971_*988delinsGCTTCACAATAAACGGCT	NP_001254483.1:n.*971_*988delinsGCTTCACAATAAACGGCT
NM_019616.3:c.*971_*988delinsGCTTCACAATAAACGGCT , LRG_554t2:c.*971_*988delinsGCTTCACAATAAACGGCT	NP_062562.1:n.*971_*988delinsGCTTCACAATAAACGGCT
NR_051961.1:n.2393_2410delinsGCTTCACAATAAACGGCT
XM_006719963.2:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_006720026.1:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537474.1:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535776.1:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537475.1:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535777.1:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537476.1:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535778.1:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537477.1:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535779.1:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_006719963.3:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_006720026.2:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537474.2:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535776.2:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537475.2:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535777.2:n.*971_*988delinsGCTTCACAATAAACGGCT
XM_011537476.2:c.*971_*988delinsGCTTCACAATAAACGGCT	XP_011535778.1:n.*971_*988delinsGCTTCACAATAAACGGCT
NM_019616.4:c.*971_*988delinsGCTTCACAATAAACGGCT MANE Select	NP_062562.1:n.*971_*988delinsGCTTCACAATAAACGGCT
NR_051961.2:n.2390_2407delinsGCTTCACAATAAACGGCT
NM_001267554.2:c.*971_*988delinsGCTTCACAATAAACGGCT	NP_001254483.1:n.*971_*988delinsGCTTCACAATAAACGGCT