Canonical Allele Identifier: CA2120144225

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119602_113119604delinsCAT , CM000675.2:g.113119602_113119604delinsCAT	GRCh38
NC_000013.10:g.113773916_113773918delinsCAT , CM000675.1:g.113773916_113773918delinsCAT	GRCh37
NC_000013.9:g.112821917_112821919delinsCAT	NCBI36
NG_009258.1:g.1804_1806delinsCAT , LRG_548:g.1804_1806delinsCAT
NG_009262.1:g.18812_18814delinsCAT , LRG_554:g.18812_18814delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*594_*596delinsCAT MANE Select	ENSP00000329546.4:n.*594_*596delinsCAT
ENST00000346342.7:c.*594_*596delinsCAT	ENSP00000329546.3:n.*594_*596delinsCAT
ENST00000375581.3:c.*594_*596delinsCAT	ENSP00000364731.3:n.*594_*596delinsCAT
ENST00000541084.5:c.*594_*596delinsCAT	ENSP00000442051.2:n.*594_*596delinsCAT
NM_000131.4:c.*594_*596delinsCAT , LRG_554t1:c.*594_*596delinsCAT	NP_000122.1:n.*594_*596delinsCAT
NM_001267554.1:c.*594_*596delinsCAT	NP_001254483.1:n.*594_*596delinsCAT
NM_019616.3:c.*594_*596delinsCAT , LRG_554t2:c.*594_*596delinsCAT	NP_062562.1:n.*594_*596delinsCAT
NR_051961.1:n.2016_2018delinsCAT
XM_006719963.2:c.*594_*596delinsCAT	XP_006720026.1:n.*594_*596delinsCAT
XM_011537474.1:c.*594_*596delinsCAT	XP_011535776.1:n.*594_*596delinsCAT
XM_011537475.1:c.*594_*596delinsCAT	XP_011535777.1:n.*594_*596delinsCAT
XM_011537476.1:c.*594_*596delinsCAT	XP_011535778.1:n.*594_*596delinsCAT
XM_011537477.1:c.*594_*596delinsCAT	XP_011535779.1:n.*594_*596delinsCAT
XM_006719963.3:c.*594_*596delinsCAT	XP_006720026.2:n.*594_*596delinsCAT
XM_011537474.2:c.*594_*596delinsCAT	XP_011535776.2:n.*594_*596delinsCAT
XM_011537475.2:c.*594_*596delinsCAT	XP_011535777.2:n.*594_*596delinsCAT
XM_011537476.2:c.*594_*596delinsCAT	XP_011535778.1:n.*594_*596delinsCAT
NM_019616.4:c.*594_*596delinsCAT MANE Select	NP_062562.1:n.*594_*596delinsCAT
NR_051961.2:n.2013_2015delinsCAT
NM_001267554.2:c.*594_*596delinsCAT	NP_001254483.1:n.*594_*596delinsCAT