Canonical Allele Identifier: CA388786457

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773071A>T (hg19) ; chr13:g.113118757A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118757A>T , CM000675.2:g.113118757A>T	GRCh38
NC_000013.10:g.113773071A>T , CM000675.1:g.113773071A>T	GRCh37
NC_000013.9:g.112821072A>T	NCBI36
NG_009258.1:g.959A>T , LRG_548:g.959A>T
NG_009262.1:g.17967A>T , LRG_554:g.17967A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1084A>T MANE Select	ENSP00000329546.4:p.Thr362Ser
ENST00000346342.7:c.1084A>T	ENSP00000329546.3:p.Thr362Ser
ENST00000375581.3:c.1150A>T	ENSP00000364731.3:p.Thr384Ser
ENST00000541084.5:c.898A>T	ENSP00000442051.2:p.Thr300Ser
NM_000131.4:c.1150A>T , LRG_554t1:c.1150A>T	NP_000122.1:p.Thr384Ser
NM_001267554.1:c.898A>T	NP_001254483.1:p.Thr300Ser
NM_019616.3:c.1084A>T , LRG_554t2:c.1084A>T	NP_062562.1:p.Thr362Ser
NR_051961.1:n.1171A>T
XM_006719963.2:c.943A>T	XP_006720026.1:p.Thr315Ser
XM_011537474.1:c.1192A>T	XP_011535776.1:p.Thr398Ser
XM_011537475.1:c.1006A>T	XP_011535777.1:p.Thr336Ser
XM_011537476.1:c.844A>T	XP_011535778.1:p.Thr282Ser
XM_011537477.1:c.1153A>T	XP_011535779.1:p.Thr385Ser
XM_006719963.3:c.988A>T	XP_006720026.2:p.Thr330Ser
XM_011537474.2:c.1237A>T	XP_011535776.2:p.Thr413Ser
XM_011537475.2:c.1051A>T	XP_011535777.2:p.Thr351Ser
XM_011537476.2:c.844A>T	XP_011535778.1:p.Thr282Ser
NM_019616.4:c.1084A>T MANE Select	NP_062562.1:p.Thr362Ser
NR_051961.2:n.1168A>T
NM_001267554.2:c.898A>T	NP_001254483.1:p.Thr300Ser