Canonical Allele Identifier: CA388785902

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772795A>C (hg19) ; chr13:g.113118481A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118481A>C , CM000675.2:g.113118481A>C	GRCh38
NC_000013.10:g.113772795A>C , CM000675.1:g.113772795A>C	GRCh37
NC_000013.9:g.112820796A>C	NCBI36
NG_009258.1:g.683A>C , LRG_548:g.683A>C
NG_009262.1:g.17691A>C , LRG_554:g.17691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.808A>C MANE Select	ENSP00000329546.4:p.Ser270Arg
ENST00000346342.7:c.808A>C	ENSP00000329546.3:p.Ser270Arg
ENST00000375581.3:c.874A>C	ENSP00000364731.3:p.Ser292Arg
ENST00000541084.5:c.622A>C	ENSP00000442051.2:p.Ser208Arg
NM_000131.4:c.874A>C , LRG_554t1:c.874A>C	NP_000122.1:p.Ser292Arg
NM_001267554.1:c.622A>C	NP_001254483.1:p.Ser208Arg
NM_019616.3:c.808A>C , LRG_554t2:c.808A>C	NP_062562.1:p.Ser270Arg
NR_051961.1:n.895A>C
XM_006719963.2:c.667A>C	XP_006720026.1:p.Ser223Arg
XM_011537474.1:c.916A>C	XP_011535776.1:p.Ser306Arg
XM_011537475.1:c.730A>C	XP_011535777.1:p.Ser244Arg
XM_011537476.1:c.568A>C	XP_011535778.1:p.Ser190Arg
XM_011537477.1:c.877A>C	XP_011535779.1:p.Ser293Arg
XM_006719963.3:c.712A>C	XP_006720026.2:p.Ser238Arg
XM_011537474.2:c.961A>C	XP_011535776.2:p.Ser321Arg
XM_011537475.2:c.775A>C	XP_011535777.2:p.Ser259Arg
XM_011537476.2:c.568A>C	XP_011535778.1:p.Ser190Arg
NM_019616.4:c.808A>C MANE Select	NP_062562.1:p.Ser270Arg
NR_051961.2:n.892A>C
NM_001267554.2:c.622A>C	NP_001254483.1:p.Ser208Arg