Canonical Allele Identifier: CA2120136031

Gene: F7

Linked Data

• dbSNP Id: rs1595075627

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114148G>A , CM000675.2:g.113114148G>A	GRCh38
NC_000013.10:g.113768462G>A , CM000675.1:g.113768462G>A	GRCh37
NC_000013.9:g.112816463G>A	NCBI36
NG_009262.1:g.13358G>A , LRG_554:g.13358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+188G>A MANE Select	ENSP00000329546.4:n.364+188G>A
ENST00000346342.7:c.364+188G>A	ENSP00000329546.3:n.364+188G>A
ENST00000375581.3:c.430+188G>A	ENSP00000364731.3:n.430+188G>A
ENST00000444337.1:c.*172+188G>A	ENSP00000387669.1:n.*172+188G>A
ENST00000473085.1:n.311+188G>A
ENST00000479674.1:n.697+188G>A
ENST00000541084.5:c.178+188G>A	ENSP00000442051.2:n.178+188G>A
NM_000131.4:c.430+188G>A , LRG_554t1:c.430+188G>A	NP_000122.1:n.430+188G>A
NM_001267554.1:c.178+188G>A	NP_001254483.1:n.178+188G>A
NM_019616.3:c.364+188G>A , LRG_554t2:c.364+188G>A	NP_062562.1:n.364+188G>A
NR_051961.1:n.451+188G>A
XM_006719963.2:c.364+188G>A	XP_006720026.1:n.364+188G>A
XM_011537474.1:c.364+188G>A	XP_011535776.1:n.364+188G>A
XM_011537475.1:c.178+188G>A	XP_011535777.1:n.178+188G>A
XM_011537477.1:c.325+188G>A	XP_011535779.1:n.325+188G>A
XM_006719963.3:c.409+188G>A	XP_006720026.2:n.409+188G>A
XM_011537474.2:c.409+188G>A	XP_011535776.2:n.409+188G>A
XM_011537475.2:c.223+188G>A	XP_011535777.2:n.223+188G>A
XM_011537476.2:c.-621G>A	XP_011535778.1:n.-621G>A
NM_019616.4:c.364+188G>A MANE Select	NP_062562.1:n.364+188G>A
NR_051961.2:n.448+188G>A
NM_001267554.2:c.178+188G>A	NP_001254483.1:n.178+188G>A