Canonical Allele Identifier: CA485423827

Gene: F7

Linked Data

• COSMIC: COSM5965540 ; COSM5965541
• MyVariant Identifiers: chr13:g.113772764G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118450G>A , CM000675.2:g.113118450G>A	GRCh38
NC_000013.10:g.113772764G>A , CM000675.1:g.113772764G>A	GRCh37
NC_000013.9:g.112820765G>A	NCBI36
NG_009258.1:g.652G>A , LRG_548:g.652G>A
NG_009262.1:g.17660G>A , LRG_554:g.17660G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.777G>A MANE Select	ENSP00000329546.4:p.Gln259=
ENST00000346342.7:c.777G>A	ENSP00000329546.3:p.Gln259=
ENST00000375581.3:c.843G>A	ENSP00000364731.3:p.Gln281=
ENST00000541084.5:c.591G>A	ENSP00000442051.2:p.Gln197=
NM_000131.4:c.843G>A , LRG_554t1:c.843G>A	NP_000122.1:p.Gln281=
NM_001267554.1:c.591G>A	NP_001254483.1:p.Gln197=
NM_019616.3:c.777G>A , LRG_554t2:c.777G>A	NP_062562.1:p.Gln259=
NR_051961.1:n.864G>A
XM_006719963.2:c.636G>A	XP_006720026.1:p.Gln212=
XM_011537474.1:c.885G>A	XP_011535776.1:p.Gln295=
XM_011537475.1:c.699G>A	XP_011535777.1:p.Gln233=
XM_011537476.1:c.537G>A	XP_011535778.1:p.Gln179=
XM_011537477.1:c.846G>A	XP_011535779.1:p.Gln282=
XM_006719963.3:c.681G>A	XP_006720026.2:p.Gln227=
XM_011537474.2:c.930G>A	XP_011535776.2:p.Gln310=
XM_011537475.2:c.744G>A	XP_011535777.2:p.Gln248=
XM_011537476.2:c.537G>A	XP_011535778.1:p.Gln179=
NM_019616.4:c.777G>A MANE Select	NP_062562.1:p.Gln259=
NR_051961.2:n.861G>A
NM_001267554.2:c.591G>A	NP_001254483.1:p.Gln197=