Canonical Allele Identifier: CA485020402

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768249C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113935C>T , CM000675.2:g.113113935C>T	GRCh38
NC_000013.10:g.113768249C>T , CM000675.1:g.113768249C>T	GRCh37
NC_000013.9:g.112816250C>T	NCBI36
NG_009262.1:g.13145C>T , LRG_554:g.13145C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.339C>T MANE Select	ENSP00000329546.4:p.Ala113=
ENST00000346342.7:c.339C>T	ENSP00000329546.3:p.Ala113=
ENST00000375581.3:c.405C>T	ENSP00000364731.3:p.Ala135=
ENST00000444337.1:c.*147C>T	ENSP00000387669.1:n.*147C>T
ENST00000473085.1:n.286C>T
ENST00000479674.1:n.672C>T
ENST00000541084.5:c.153C>T	ENSP00000442051.2:p.Ala51=
NM_000131.4:c.405C>T , LRG_554t1:c.405C>T	NP_000122.1:p.Ala135=
NM_001267554.1:c.153C>T	NP_001254483.1:p.Ala51=
NM_019616.3:c.339C>T , LRG_554t2:c.339C>T	NP_062562.1:p.Ala113=
NR_051961.1:n.426C>T
XM_006719963.2:c.339C>T	XP_006720026.1:p.Ala113=
XM_011537474.1:c.339C>T	XP_011535776.1:p.Ala113=
XM_011537475.1:c.153C>T	XP_011535777.1:p.Ala51=
XM_011537477.1:c.300C>T	XP_011535779.1:p.Ala100=
XM_006719963.3:c.384C>T	XP_006720026.2:p.Ala128=
XM_011537474.2:c.384C>T	XP_011535776.2:p.Ala128=
XM_011537475.2:c.198C>T	XP_011535777.2:p.Ala66=
NM_019616.4:c.339C>T MANE Select	NP_062562.1:p.Ala113=
NR_051961.2:n.423C>T
NM_001267554.2:c.153C>T	NP_001254483.1:p.Ala51=