Canonical Allele Identifier: CA388786172

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772936T>A (hg19) ; chr13:g.113118622T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118622T>A , CM000675.2:g.113118622T>A	GRCh38
NC_000013.10:g.113772936T>A , CM000675.1:g.113772936T>A	GRCh37
NC_000013.9:g.112820937T>A	NCBI36
NG_009258.1:g.824T>A , LRG_548:g.824T>A
NG_009262.1:g.17832T>A , LRG_554:g.17832T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.949T>A MANE Select	ENSP00000329546.4:p.Ser317Thr
ENST00000346342.7:c.949T>A	ENSP00000329546.3:p.Ser317Thr
ENST00000375581.3:c.1015T>A	ENSP00000364731.3:p.Ser339Thr
ENST00000541084.5:c.763T>A	ENSP00000442051.2:p.Ser255Thr
NM_000131.4:c.1015T>A , LRG_554t1:c.1015T>A	NP_000122.1:p.Ser339Thr
NM_001267554.1:c.763T>A	NP_001254483.1:p.Ser255Thr
NM_019616.3:c.949T>A , LRG_554t2:c.949T>A	NP_062562.1:p.Ser317Thr
NR_051961.1:n.1036T>A
XM_006719963.2:c.808T>A	XP_006720026.1:p.Ser270Thr
XM_011537474.1:c.1057T>A	XP_011535776.1:p.Ser353Thr
XM_011537475.1:c.871T>A	XP_011535777.1:p.Ser291Thr
XM_011537476.1:c.709T>A	XP_011535778.1:p.Ser237Thr
XM_011537477.1:c.1018T>A	XP_011535779.1:p.Ser340Thr
XM_006719963.3:c.853T>A	XP_006720026.2:p.Ser285Thr
XM_011537474.2:c.1102T>A	XP_011535776.2:p.Ser368Thr
XM_011537475.2:c.916T>A	XP_011535777.2:p.Ser306Thr
XM_011537476.2:c.709T>A	XP_011535778.1:p.Ser237Thr
NM_019616.4:c.949T>A MANE Select	NP_062562.1:p.Ser317Thr
NR_051961.2:n.1033T>A
NM_001267554.2:c.763T>A	NP_001254483.1:p.Ser255Thr