Canonical Allele Identifier: CA2575461720

Gene: F7

Linked Data

• gnomAD v4: 13-113118342-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118342C>T , CM000675.2:g.113118342C>T	GRCh38
NC_000013.10:g.113772656C>T , CM000675.1:g.113772656C>T	GRCh37
NC_000013.9:g.112820657C>T	NCBI36
NG_009258.1:g.544C>T , LRG_548:g.544C>T
NG_009262.1:g.17552C>T , LRG_554:g.17552C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.740-71C>T MANE Select	ENSP00000329546.4:n.740-71C>T
ENST00000346342.7:c.740-71C>T	ENSP00000329546.3:n.740-71C>T
ENST00000375581.3:c.806-71C>T	ENSP00000364731.3:n.806-71C>T
ENST00000541084.5:c.554-71C>T	ENSP00000442051.2:n.554-71C>T
NM_000131.4:c.806-71C>T , LRG_554t1:c.806-71C>T	NP_000122.1:n.806-71C>T
NM_001267554.1:c.554-71C>T	NP_001254483.1:n.554-71C>T
NM_019616.3:c.740-71C>T , LRG_554t2:c.740-71C>T	NP_062562.1:n.740-71C>T
NR_051961.1:n.827-71C>T
XM_006719963.2:c.599-71C>T	XP_006720026.1:n.599-71C>T
XM_011537474.1:c.848-71C>T	XP_011535776.1:n.848-71C>T
XM_011537475.1:c.662-71C>T	XP_011535777.1:n.662-71C>T
XM_011537476.1:c.500-71C>T	XP_011535778.1:n.500-71C>T
XM_011537477.1:c.809-71C>T	XP_011535779.1:n.809-71C>T
XM_006719963.3:c.644-71C>T	XP_006720026.2:n.644-71C>T
XM_011537474.2:c.893-71C>T	XP_011535776.2:n.893-71C>T
XM_011537475.2:c.707-71C>T	XP_011535777.2:n.707-71C>T
XM_011537476.2:c.500-71C>T	XP_011535778.1:n.500-71C>T
NM_019616.4:c.740-71C>T MANE Select	NP_062562.1:n.740-71C>T
NR_051961.2:n.824-71C>T
NM_001267554.2:c.554-71C>T	NP_001254483.1:n.554-71C>T