Canonical Allele Identifier: CA388786773

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773137G>T (hg19) ; chr13:g.113118823G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118823G>T , CM000675.2:g.113118823G>T	GRCh38
NC_000013.10:g.113773137G>T , CM000675.1:g.113773137G>T	GRCh37
NC_000013.9:g.112821138G>T	NCBI36
NG_009258.1:g.1025G>T , LRG_548:g.1025G>T
NG_009262.1:g.18033G>T , LRG_554:g.18033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1150G>T MANE Select	ENSP00000329546.4:p.Gly384Cys
ENST00000346342.7:c.1150G>T	ENSP00000329546.3:p.Gly384Cys
ENST00000375581.3:c.1216G>T	ENSP00000364731.3:p.Gly406Cys
ENST00000541084.5:c.964G>T	ENSP00000442051.2:p.Gly322Cys
NM_000131.4:c.1216G>T , LRG_554t1:c.1216G>T	NP_000122.1:p.Gly406Cys
NM_001267554.1:c.964G>T	NP_001254483.1:p.Gly322Cys
NM_019616.3:c.1150G>T , LRG_554t2:c.1150G>T	NP_062562.1:p.Gly384Cys
NR_051961.1:n.1237G>T
XM_006719963.2:c.1009G>T	XP_006720026.1:p.Gly337Cys
XM_011537474.1:c.1258G>T	XP_011535776.1:p.Gly420Cys
XM_011537475.1:c.1072G>T	XP_011535777.1:p.Gly358Cys
XM_011537476.1:c.910G>T	XP_011535778.1:p.Gly304Cys
XM_011537477.1:c.1219G>T	XP_011535779.1:p.Gly407Cys
XM_006719963.3:c.1054G>T	XP_006720026.2:p.Gly352Cys
XM_011537474.2:c.1303G>T	XP_011535776.2:p.Gly435Cys
XM_011537475.2:c.1117G>T	XP_011535777.2:p.Gly373Cys
XM_011537476.2:c.910G>T	XP_011535778.1:p.Gly304Cys
NM_019616.4:c.1150G>T MANE Select	NP_062562.1:p.Gly384Cys
NR_051961.2:n.1234G>T
NM_001267554.2:c.964G>T	NP_001254483.1:p.Gly322Cys