Canonical Allele Identifier: CA485021205

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773148C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118834C>T , CM000675.2:g.113118834C>T	GRCh38
NC_000013.10:g.113773148C>T , CM000675.1:g.113773148C>T	GRCh37
NC_000013.9:g.112821149C>T	NCBI36
NG_009258.1:g.1036C>T , LRG_548:g.1036C>T
NG_009262.1:g.18044C>T , LRG_554:g.18044C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1161C>T MANE Select	ENSP00000329546.4:p.Ala387=
ENST00000346342.7:c.1161C>T	ENSP00000329546.3:p.Ala387=
ENST00000375581.3:c.1227C>T	ENSP00000364731.3:p.Ala409=
ENST00000541084.5:c.975C>T	ENSP00000442051.2:p.Ala325=
NM_000131.4:c.1227C>T , LRG_554t1:c.1227C>T	NP_000122.1:p.Ala409=
NM_001267554.1:c.975C>T	NP_001254483.1:p.Ala325=
NM_019616.3:c.1161C>T , LRG_554t2:c.1161C>T	NP_062562.1:p.Ala387=
NR_051961.1:n.1248C>T
XM_006719963.2:c.1020C>T	XP_006720026.1:p.Ala340=
XM_011537474.1:c.1269C>T	XP_011535776.1:p.Ala423=
XM_011537475.1:c.1083C>T	XP_011535777.1:p.Ala361=
XM_011537476.1:c.921C>T	XP_011535778.1:p.Ala307=
XM_011537477.1:c.1230C>T	XP_011535779.1:p.Ala410=
XM_006719963.3:c.1065C>T	XP_006720026.2:p.Ala355=
XM_011537474.2:c.1314C>T	XP_011535776.2:p.Ala438=
XM_011537475.2:c.1128C>T	XP_011535777.2:p.Ala376=
XM_011537476.2:c.921C>T	XP_011535778.1:p.Ala307=
NM_019616.4:c.1161C>T MANE Select	NP_062562.1:p.Ala387=
NR_051961.2:n.1245C>T
NM_001267554.2:c.975C>T	NP_001254483.1:p.Ala325=