Canonical Allele Identifier: CA485423935

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772920G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118606G>A , CM000675.2:g.113118606G>A	GRCh38
NC_000013.10:g.113772920G>A , CM000675.1:g.113772920G>A	GRCh37
NC_000013.9:g.112820921G>A	NCBI36
NG_009258.1:g.808G>A , LRG_548:g.808G>A
NG_009262.1:g.17816G>A , LRG_554:g.17816G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.933G>A MANE Select	ENSP00000329546.4:p.Leu311=
ENST00000346342.7:c.933G>A	ENSP00000329546.3:p.Leu311=
ENST00000375581.3:c.999G>A	ENSP00000364731.3:p.Leu333=
ENST00000541084.5:c.747G>A	ENSP00000442051.2:p.Leu249=
NM_000131.4:c.999G>A , LRG_554t1:c.999G>A	NP_000122.1:p.Leu333=
NM_001267554.1:c.747G>A	NP_001254483.1:p.Leu249=
NM_019616.3:c.933G>A , LRG_554t2:c.933G>A	NP_062562.1:p.Leu311=
NR_051961.1:n.1020G>A
XM_006719963.2:c.792G>A	XP_006720026.1:p.Leu264=
XM_011537474.1:c.1041G>A	XP_011535776.1:p.Leu347=
XM_011537475.1:c.855G>A	XP_011535777.1:p.Leu285=
XM_011537476.1:c.693G>A	XP_011535778.1:p.Leu231=
XM_011537477.1:c.1002G>A	XP_011535779.1:p.Leu334=
XM_006719963.3:c.837G>A	XP_006720026.2:p.Leu279=
XM_011537474.2:c.1086G>A	XP_011535776.2:p.Leu362=
XM_011537475.2:c.900G>A	XP_011535777.2:p.Leu300=
XM_011537476.2:c.693G>A	XP_011535778.1:p.Leu231=
NM_019616.4:c.933G>A MANE Select	NP_062562.1:p.Leu311=
NR_051961.2:n.1017G>A
NM_001267554.2:c.747G>A	NP_001254483.1:p.Leu249=