Canonical Allele Identifier: CA485423835

Gene: F7

Linked Data

• gnomAD v4: 13-113118459-G-T
• MyVariant Identifiers: chr13:g.113772773G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118459G>T , CM000675.2:g.113118459G>T	GRCh38
NC_000013.10:g.113772773G>T , CM000675.1:g.113772773G>T	GRCh37
NC_000013.9:g.112820774G>T	NCBI36
NG_009258.1:g.661G>T , LRG_548:g.661G>T
NG_009262.1:g.17669G>T , LRG_554:g.17669G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.786G>T MANE Select	ENSP00000329546.4:p.Arg262=
ENST00000346342.7:c.786G>T	ENSP00000329546.3:p.Arg262=
ENST00000375581.3:c.852G>T	ENSP00000364731.3:p.Arg284=
ENST00000541084.5:c.600G>T	ENSP00000442051.2:p.Arg200=
NM_000131.4:c.852G>T , LRG_554t1:c.852G>T	NP_000122.1:p.Arg284=
NM_001267554.1:c.600G>T	NP_001254483.1:p.Arg200=
NM_019616.3:c.786G>T , LRG_554t2:c.786G>T	NP_062562.1:p.Arg262=
NR_051961.1:n.873G>T
XM_006719963.2:c.645G>T	XP_006720026.1:p.Arg215=
XM_011537474.1:c.894G>T	XP_011535776.1:p.Arg298=
XM_011537475.1:c.708G>T	XP_011535777.1:p.Arg236=
XM_011537476.1:c.546G>T	XP_011535778.1:p.Arg182=
XM_011537477.1:c.855G>T	XP_011535779.1:p.Arg285=
XM_006719963.3:c.690G>T	XP_006720026.2:p.Arg230=
XM_011537474.2:c.939G>T	XP_011535776.2:p.Arg313=
XM_011537475.2:c.753G>T	XP_011535777.2:p.Arg251=
XM_011537476.2:c.546G>T	XP_011535778.1:p.Arg182=
NM_019616.4:c.786G>T MANE Select	NP_062562.1:p.Arg262=
NR_051961.2:n.870G>T
NM_001267554.2:c.600G>T	NP_001254483.1:p.Arg200=