Canonical Allele Identifier: CA2503187700

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118228C>A , CM000675.2:g.113118228C>A	GRCh38
NC_000013.10:g.113772542C>A , CM000675.1:g.113772542C>A	GRCh37
NC_000013.9:g.112820543C>A	NCBI36
NG_009258.1:g.430C>A , LRG_548:g.430C>A
NG_009262.1:g.17438C>A , LRG_554:g.17438C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.740-185C>A MANE Select	ENSP00000329546.4:n.740-185C>A
ENST00000346342.7:c.740-185C>A	ENSP00000329546.3:n.740-185C>A
ENST00000375581.3:c.806-185C>A	ENSP00000364731.3:n.806-185C>A
ENST00000541084.5:c.554-185C>A	ENSP00000442051.2:n.554-185C>A
NM_000131.4:c.806-185C>A , LRG_554t1:c.806-185C>A	NP_000122.1:n.806-185C>A
NM_001267554.1:c.554-185C>A	NP_001254483.1:n.554-185C>A
NM_019616.3:c.740-185C>A , LRG_554t2:c.740-185C>A	NP_062562.1:n.740-185C>A
NR_051961.1:n.827-185C>A
XM_006719963.2:c.599-185C>A	XP_006720026.1:n.599-185C>A
XM_011537474.1:c.848-185C>A	XP_011535776.1:n.848-185C>A
XM_011537475.1:c.662-185C>A	XP_011535777.1:n.662-185C>A
XM_011537476.1:c.500-185C>A	XP_011535778.1:n.500-185C>A
XM_011537477.1:c.809-185C>A	XP_011535779.1:n.809-185C>A
XM_006719963.3:c.644-185C>A	XP_006720026.2:n.644-185C>A
XM_011537474.2:c.893-185C>A	XP_011535776.2:n.893-185C>A
XM_011537475.2:c.707-185C>A	XP_011535777.2:n.707-185C>A
XM_011537476.2:c.500-185C>A	XP_011535778.1:n.500-185C>A
NM_019616.4:c.740-185C>A MANE Select	NP_062562.1:n.740-185C>A
NR_051961.2:n.824-185C>A
NM_001267554.2:c.554-185C>A	NP_001254483.1:n.554-185C>A