Canonical Allele Identifier: CA388785934

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772813A>T (hg19) ; chr13:g.113118499A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118499A>T , CM000675.2:g.113118499A>T	GRCh38
NC_000013.10:g.113772813A>T , CM000675.1:g.113772813A>T	GRCh37
NC_000013.9:g.112820814A>T	NCBI36
NG_009258.1:g.701A>T , LRG_548:g.701A>T
NG_009262.1:g.17709A>T , LRG_554:g.17709A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.826A>T MANE Select	ENSP00000329546.4:p.Thr276Ser
ENST00000346342.7:c.826A>T	ENSP00000329546.3:p.Thr276Ser
ENST00000375581.3:c.892A>T	ENSP00000364731.3:p.Thr298Ser
ENST00000541084.5:c.640A>T	ENSP00000442051.2:p.Thr214Ser
NM_000131.4:c.892A>T , LRG_554t1:c.892A>T	NP_000122.1:p.Thr298Ser
NM_001267554.1:c.640A>T	NP_001254483.1:p.Thr214Ser
NM_019616.3:c.826A>T , LRG_554t2:c.826A>T	NP_062562.1:p.Thr276Ser
NR_051961.1:n.913A>T
XM_006719963.2:c.685A>T	XP_006720026.1:p.Thr229Ser
XM_011537474.1:c.934A>T	XP_011535776.1:p.Thr312Ser
XM_011537475.1:c.748A>T	XP_011535777.1:p.Thr250Ser
XM_011537476.1:c.586A>T	XP_011535778.1:p.Thr196Ser
XM_011537477.1:c.895A>T	XP_011535779.1:p.Thr299Ser
XM_006719963.3:c.730A>T	XP_006720026.2:p.Thr244Ser
XM_011537474.2:c.979A>T	XP_011535776.2:p.Thr327Ser
XM_011537475.2:c.793A>T	XP_011535777.2:p.Thr265Ser
XM_011537476.2:c.586A>T	XP_011535778.1:p.Thr196Ser
NM_019616.4:c.826A>T MANE Select	NP_062562.1:p.Thr276Ser
NR_051961.2:n.910A>T
NM_001267554.2:c.640A>T	NP_001254483.1:p.Thr214Ser