Canonical Allele Identifier: CA388785987

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772840C>A (hg19) ; chr13:g.113118526C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118526C>A , CM000675.2:g.113118526C>A	GRCh38
NC_000013.10:g.113772840C>A , CM000675.1:g.113772840C>A	GRCh37
NC_000013.9:g.112820841C>A	NCBI36
NG_009258.1:g.728C>A , LRG_548:g.728C>A
NG_009262.1:g.17736C>A , LRG_554:g.17736C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.853C>A MANE Select	ENSP00000329546.4:p.Arg285Ser
ENST00000346342.7:c.853C>A	ENSP00000329546.3:p.Arg285Ser
ENST00000375581.3:c.919C>A	ENSP00000364731.3:p.Arg307Ser
ENST00000541084.5:c.667C>A	ENSP00000442051.2:p.Arg223Ser
NM_000131.4:c.919C>A , LRG_554t1:c.919C>A	NP_000122.1:p.Arg307Ser
NM_001267554.1:c.667C>A	NP_001254483.1:p.Arg223Ser
NM_019616.3:c.853C>A , LRG_554t2:c.853C>A	NP_062562.1:p.Arg285Ser
NR_051961.1:n.940C>A
XM_006719963.2:c.712C>A	XP_006720026.1:p.Arg238Ser
XM_011537474.1:c.961C>A	XP_011535776.1:p.Arg321Ser
XM_011537475.1:c.775C>A	XP_011535777.1:p.Arg259Ser
XM_011537476.1:c.613C>A	XP_011535778.1:p.Arg205Ser
XM_011537477.1:c.922C>A	XP_011535779.1:p.Arg308Ser
XM_006719963.3:c.757C>A	XP_006720026.2:p.Arg253Ser
XM_011537474.2:c.1006C>A	XP_011535776.2:p.Arg336Ser
XM_011537475.2:c.820C>A	XP_011535777.2:p.Arg274Ser
XM_011537476.2:c.613C>A	XP_011535778.1:p.Arg205Ser
NM_019616.4:c.853C>A MANE Select	NP_062562.1:p.Arg285Ser
NR_051961.2:n.937C>A
NM_001267554.2:c.667C>A	NP_001254483.1:p.Arg223Ser