Canonical Allele Identifier: CA388786190

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772945A>C (hg19) ; chr13:g.113118631A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118631A>C , CM000675.2:g.113118631A>C	GRCh38
NC_000013.10:g.113772945A>C , CM000675.1:g.113772945A>C	GRCh37
NC_000013.9:g.112820946A>C	NCBI36
NG_009258.1:g.833A>C , LRG_548:g.833A>C
NG_009262.1:g.17841A>C , LRG_554:g.17841A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.958A>C MANE Select	ENSP00000329546.4:p.Ser320Arg
ENST00000346342.7:c.958A>C	ENSP00000329546.3:p.Ser320Arg
ENST00000375581.3:c.1024A>C	ENSP00000364731.3:p.Ser342Arg
ENST00000541084.5:c.772A>C	ENSP00000442051.2:p.Ser258Arg
NM_000131.4:c.1024A>C , LRG_554t1:c.1024A>C	NP_000122.1:p.Ser342Arg
NM_001267554.1:c.772A>C	NP_001254483.1:p.Ser258Arg
NM_019616.3:c.958A>C , LRG_554t2:c.958A>C	NP_062562.1:p.Ser320Arg
NR_051961.1:n.1045A>C
XM_006719963.2:c.817A>C	XP_006720026.1:p.Ser273Arg
XM_011537474.1:c.1066A>C	XP_011535776.1:p.Ser356Arg
XM_011537475.1:c.880A>C	XP_011535777.1:p.Ser294Arg
XM_011537476.1:c.718A>C	XP_011535778.1:p.Ser240Arg
XM_011537477.1:c.1027A>C	XP_011535779.1:p.Ser343Arg
XM_006719963.3:c.862A>C	XP_006720026.2:p.Ser288Arg
XM_011537474.2:c.1111A>C	XP_011535776.2:p.Ser371Arg
XM_011537475.2:c.925A>C	XP_011535777.2:p.Ser309Arg
XM_011537476.2:c.718A>C	XP_011535778.1:p.Ser240Arg
NM_019616.4:c.958A>C MANE Select	NP_062562.1:p.Ser320Arg
NR_051961.2:n.1042A>C
NM_001267554.2:c.772A>C	NP_001254483.1:p.Ser258Arg