Canonical Allele Identifier: CA388787210

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773302C>A (hg19) ; chr13:g.113118988C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118988C>A , CM000675.2:g.113118988C>A	GRCh38
NC_000013.10:g.113773302C>A , CM000675.1:g.113773302C>A	GRCh37
NC_000013.9:g.112821303C>A	NCBI36
NG_009258.1:g.1190C>A , LRG_548:g.1190C>A
NG_009262.1:g.18198C>A , LRG_554:g.18198C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1315C>A MANE Select	ENSP00000329546.4:p.Leu439Met
ENST00000346342.7:c.1315C>A	ENSP00000329546.3:p.Leu439Met
ENST00000375581.3:c.1381C>A	ENSP00000364731.3:p.Leu461Met
ENST00000541084.5:c.1129C>A	ENSP00000442051.2:p.Leu377Met
NM_000131.4:c.1381C>A , LRG_554t1:c.1381C>A	NP_000122.1:p.Leu461Met
NM_001267554.1:c.1129C>A	NP_001254483.1:p.Leu377Met
NM_019616.3:c.1315C>A , LRG_554t2:c.1315C>A	NP_062562.1:p.Leu439Met
NR_051961.1:n.1402C>A
XM_006719963.2:c.1174C>A	XP_006720026.1:p.Leu392Met
XM_011537474.1:c.1423C>A	XP_011535776.1:p.Leu475Met
XM_011537475.1:c.1237C>A	XP_011535777.1:p.Leu413Met
XM_011537476.1:c.1075C>A	XP_011535778.1:p.Leu359Met
XM_011537477.1:c.1384C>A	XP_011535779.1:p.Leu462Met
XM_006719963.3:c.1219C>A	XP_006720026.2:p.Leu407Met
XM_011537474.2:c.1468C>A	XP_011535776.2:p.Leu490Met
XM_011537475.2:c.1282C>A	XP_011535777.2:p.Leu428Met
XM_011537476.2:c.1075C>A	XP_011535778.1:p.Leu359Met
NM_019616.4:c.1315C>A MANE Select	NP_062562.1:p.Leu439Met
NR_051961.2:n.1399C>A
NM_001267554.2:c.1129C>A	NP_001254483.1:p.Leu377Met