Canonical Allele Identifier: CA2800664094

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119702_113119717del , CM000675.2:g.113119702_113119717del	GRCh38
NC_000013.10:g.113774016_113774031del , CM000675.1:g.113774016_113774031del	GRCh37
NC_000013.9:g.112822017_112822032del	NCBI36
NG_009258.1:g.1904_1919del , LRG_548:g.1904_1919del
NG_009262.1:g.18912_18927del , LRG_554:g.18912_18927del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*694_*709del MANE Select	ENSP00000329546.4:n.*694_*709del
ENST00000346342.7:c.*694_*709del	ENSP00000329546.3:n.*694_*709del
ENST00000375581.3:c.*694_*709del	ENSP00000364731.3:n.*694_*709del
ENST00000541084.5:c.*694_*709del	ENSP00000442051.2:n.*694_*709del
NM_000131.4:c.*694_*709del , LRG_554t1:c.*694_*709del	NP_000122.1:n.*694_*709del
NM_001267554.1:c.*694_*709del	NP_001254483.1:n.*694_*709del
NM_019616.3:c.*694_*709del , LRG_554t2:c.*694_*709del	NP_062562.1:n.*694_*709del
NR_051961.1:n.2116_2131del
XM_006719963.2:c.*694_*709del	XP_006720026.1:n.*694_*709del
XM_011537474.1:c.*694_*709del	XP_011535776.1:n.*694_*709del
XM_011537475.1:c.*694_*709del	XP_011535777.1:n.*694_*709del
XM_011537476.1:c.*694_*709del	XP_011535778.1:n.*694_*709del
XM_011537477.1:c.*694_*709del	XP_011535779.1:n.*694_*709del
XM_006719963.3:c.*694_*709del	XP_006720026.2:n.*694_*709del
XM_011537474.2:c.*694_*709del	XP_011535776.2:n.*694_*709del
XM_011537475.2:c.*694_*709del	XP_011535777.2:n.*694_*709del
XM_011537476.2:c.*694_*709del	XP_011535778.1:n.*694_*709del
NM_019616.4:c.*694_*709del MANE Select	NP_062562.1:n.*694_*709del
NR_051961.2:n.2113_2128del
NM_001267554.2:c.*694_*709del	NP_001254483.1:n.*694_*709del