Canonical Allele Identifier: CA485423872

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772833G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118519G>T , CM000675.2:g.113118519G>T	GRCh38
NC_000013.10:g.113772833G>T , CM000675.1:g.113772833G>T	GRCh37
NC_000013.9:g.112820834G>T	NCBI36
NG_009258.1:g.721G>T , LRG_548:g.721G>T
NG_009262.1:g.17729G>T , LRG_554:g.17729G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.846G>T MANE Select	ENSP00000329546.4:p.Ala282=
ENST00000346342.7:c.846G>T	ENSP00000329546.3:p.Ala282=
ENST00000375581.3:c.912G>T	ENSP00000364731.3:p.Ala304=
ENST00000541084.5:c.660G>T	ENSP00000442051.2:p.Ala220=
NM_000131.4:c.912G>T , LRG_554t1:c.912G>T	NP_000122.1:p.Ala304=
NM_001267554.1:c.660G>T	NP_001254483.1:p.Ala220=
NM_019616.3:c.846G>T , LRG_554t2:c.846G>T	NP_062562.1:p.Ala282=
NR_051961.1:n.933G>T
XM_006719963.2:c.705G>T	XP_006720026.1:p.Ala235=
XM_011537474.1:c.954G>T	XP_011535776.1:p.Ala318=
XM_011537475.1:c.768G>T	XP_011535777.1:p.Ala256=
XM_011537476.1:c.606G>T	XP_011535778.1:p.Ala202=
XM_011537477.1:c.915G>T	XP_011535779.1:p.Ala305=
XM_006719963.3:c.750G>T	XP_006720026.2:p.Ala250=
XM_011537474.2:c.999G>T	XP_011535776.2:p.Ala333=
XM_011537475.2:c.813G>T	XP_011535777.2:p.Ala271=
XM_011537476.2:c.606G>T	XP_011535778.1:p.Ala202=
NM_019616.4:c.846G>T MANE Select	NP_062562.1:p.Ala282=
NR_051961.2:n.930G>T
NM_001267554.2:c.660G>T	NP_001254483.1:p.Ala220=