Canonical Allele Identifier: CA388787209

Gene: F7

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1315C>G MANE Select	ENSP00000329546.4:p.Leu439Val
ENST00000346342.7:c.1315C>G	ENSP00000329546.3:p.Leu439Val
ENST00000375581.3:c.1381C>G	ENSP00000364731.3:p.Leu461Val
ENST00000541084.5:c.1129C>G	ENSP00000442051.2:p.Leu377Val
NM_000131.4:c.1381C>G , LRG_554t1:c.1381C>G	NP_000122.1:p.Leu461Val
NM_001267554.1:c.1129C>G	NP_001254483.1:p.Leu377Val
NM_019616.3:c.1315C>G , LRG_554t2:c.1315C>G	NP_062562.1:p.Leu439Val
NR_051961.1:n.1402C>G
XM_006719963.2:c.1174C>G	XP_006720026.1:p.Leu392Val
XM_011537474.1:c.1423C>G	XP_011535776.1:p.Leu475Val
XM_011537475.1:c.1237C>G	XP_011535777.1:p.Leu413Val
XM_011537476.1:c.1075C>G	XP_011535778.1:p.Leu359Val
XM_011537477.1:c.1384C>G	XP_011535779.1:p.Leu462Val
XM_006719963.3:c.1219C>G	XP_006720026.2:p.Leu407Val
XM_011537474.2:c.1468C>G	XP_011535776.2:p.Leu490Val
XM_011537475.2:c.1282C>G	XP_011535777.2:p.Leu428Val
XM_011537476.2:c.1075C>G	XP_011535778.1:p.Leu359Val
NM_019616.4:c.1315C>G MANE Select	NP_062562.1:p.Leu439Val
NR_051961.2:n.1399C>G
NM_001267554.2:c.1129C>G	NP_001254483.1:p.Leu377Val