Canonical Allele Identifier: CA485423979

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772986G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118672G>A , CM000675.2:g.113118672G>A	GRCh38
NC_000013.10:g.113772986G>A , CM000675.1:g.113772986G>A	GRCh37
NC_000013.9:g.112820987G>A	NCBI36
NG_009258.1:g.874G>A , LRG_548:g.874G>A
NG_009262.1:g.17882G>A , LRG_554:g.17882G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.999G>A MANE Select	ENSP00000329546.4:p.Leu333=
ENST00000346342.7:c.999G>A	ENSP00000329546.3:p.Leu333=
ENST00000375581.3:c.1065G>A	ENSP00000364731.3:p.Leu355=
ENST00000541084.5:c.813G>A	ENSP00000442051.2:p.Leu271=
NM_000131.4:c.1065G>A , LRG_554t1:c.1065G>A	NP_000122.1:p.Leu355=
NM_001267554.1:c.813G>A	NP_001254483.1:p.Leu271=
NM_019616.3:c.999G>A , LRG_554t2:c.999G>A	NP_062562.1:p.Leu333=
NR_051961.1:n.1086G>A
XM_006719963.2:c.858G>A	XP_006720026.1:p.Leu286=
XM_011537474.1:c.1107G>A	XP_011535776.1:p.Leu369=
XM_011537475.1:c.921G>A	XP_011535777.1:p.Leu307=
XM_011537476.1:c.759G>A	XP_011535778.1:p.Leu253=
XM_011537477.1:c.1068G>A	XP_011535779.1:p.Leu356=
XM_006719963.3:c.903G>A	XP_006720026.2:p.Leu301=
XM_011537474.2:c.1152G>A	XP_011535776.2:p.Leu384=
XM_011537475.2:c.966G>A	XP_011535777.2:p.Leu322=
XM_011537476.2:c.759G>A	XP_011535778.1:p.Leu253=
NM_019616.4:c.999G>A MANE Select	NP_062562.1:p.Leu333=
NR_051961.2:n.1083G>A
NM_001267554.2:c.813G>A	NP_001254483.1:p.Leu271=