Canonical Allele Identifier: CA485021797

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773316T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119002T>C , CM000675.2:g.113119002T>C	GRCh38
NC_000013.10:g.113773316T>C , CM000675.1:g.113773316T>C	GRCh37
NC_000013.9:g.112821317T>C	NCBI36
NG_009258.1:g.1204T>C , LRG_548:g.1204T>C
NG_009262.1:g.18212T>C , LRG_554:g.18212T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1329T>C MANE Select	ENSP00000329546.4:p.Phe443=
ENST00000346342.7:c.1329T>C	ENSP00000329546.3:p.Phe443=
ENST00000375581.3:c.1395T>C	ENSP00000364731.3:p.Phe465=
ENST00000541084.5:c.1143T>C	ENSP00000442051.2:p.Phe381=
NM_000131.4:c.1395T>C , LRG_554t1:c.1395T>C	NP_000122.1:p.Phe465=
NM_001267554.1:c.1143T>C	NP_001254483.1:p.Phe381=
NM_019616.3:c.1329T>C , LRG_554t2:c.1329T>C	NP_062562.1:p.Phe443=
NR_051961.1:n.1416T>C
XM_006719963.2:c.1188T>C	XP_006720026.1:p.Phe396=
XM_011537474.1:c.1437T>C	XP_011535776.1:p.Phe479=
XM_011537475.1:c.1251T>C	XP_011535777.1:p.Phe417=
XM_011537476.1:c.1089T>C	XP_011535778.1:p.Phe363=
XM_011537477.1:c.1398T>C	XP_011535779.1:p.Phe466=
XM_006719963.3:c.1233T>C	XP_006720026.2:p.Phe411=
XM_011537474.2:c.1482T>C	XP_011535776.2:p.Phe494=
XM_011537475.2:c.1296T>C	XP_011535777.2:p.Phe432=
XM_011537476.2:c.1089T>C	XP_011535778.1:p.Phe363=
NM_019616.4:c.1329T>C MANE Select	NP_062562.1:p.Phe443=
NR_051961.2:n.1413T>C
NM_001267554.2:c.1143T>C	NP_001254483.1:p.Phe381=