Canonical Allele Identifier: CA388786197

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772947C>G (hg19) ; chr13:g.113118633C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118633C>G , CM000675.2:g.113118633C>G	GRCh38
NC_000013.10:g.113772947C>G , CM000675.1:g.113772947C>G	GRCh37
NC_000013.9:g.112820948C>G	NCBI36
NG_009258.1:g.835C>G , LRG_548:g.835C>G
NG_009262.1:g.17843C>G , LRG_554:g.17843C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.960C>G MANE Select	ENSP00000329546.4:p.Ser320Arg
ENST00000346342.7:c.960C>G	ENSP00000329546.3:p.Ser320Arg
ENST00000375581.3:c.1026C>G	ENSP00000364731.3:p.Ser342Arg
ENST00000541084.5:c.774C>G	ENSP00000442051.2:p.Ser258Arg
NM_000131.4:c.1026C>G , LRG_554t1:c.1026C>G	NP_000122.1:p.Ser342Arg
NM_001267554.1:c.774C>G	NP_001254483.1:p.Ser258Arg
NM_019616.3:c.960C>G , LRG_554t2:c.960C>G	NP_062562.1:p.Ser320Arg
NR_051961.1:n.1047C>G
XM_006719963.2:c.819C>G	XP_006720026.1:p.Ser273Arg
XM_011537474.1:c.1068C>G	XP_011535776.1:p.Ser356Arg
XM_011537475.1:c.882C>G	XP_011535777.1:p.Ser294Arg
XM_011537476.1:c.720C>G	XP_011535778.1:p.Ser240Arg
XM_011537477.1:c.1029C>G	XP_011535779.1:p.Ser343Arg
XM_006719963.3:c.864C>G	XP_006720026.2:p.Ser288Arg
XM_011537474.2:c.1113C>G	XP_011535776.2:p.Ser371Arg
XM_011537475.2:c.927C>G	XP_011535777.2:p.Ser309Arg
XM_011537476.2:c.720C>G	XP_011535778.1:p.Ser240Arg
NM_019616.4:c.960C>G MANE Select	NP_062562.1:p.Ser320Arg
NR_051961.2:n.1044C>G
NM_001267554.2:c.774C>G	NP_001254483.1:p.Ser258Arg