Canonical Allele Identifier: CA388786132

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772914G>T (hg19) ; chr13:g.113118600G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118600G>T , CM000675.2:g.113118600G>T	GRCh38
NC_000013.10:g.113772914G>T , CM000675.1:g.113772914G>T	GRCh37
NC_000013.9:g.112820915G>T	NCBI36
NG_009258.1:g.802G>T , LRG_548:g.802G>T
NG_009262.1:g.17810G>T , LRG_554:g.17810G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.927G>T MANE Select	ENSP00000329546.4:p.Arg309Ser
ENST00000346342.7:c.927G>T	ENSP00000329546.3:p.Arg309Ser
ENST00000375581.3:c.993G>T	ENSP00000364731.3:p.Arg331Ser
ENST00000541084.5:c.741G>T	ENSP00000442051.2:p.Arg247Ser
NM_000131.4:c.993G>T , LRG_554t1:c.993G>T	NP_000122.1:p.Arg331Ser
NM_001267554.1:c.741G>T	NP_001254483.1:p.Arg247Ser
NM_019616.3:c.927G>T , LRG_554t2:c.927G>T	NP_062562.1:p.Arg309Ser
NR_051961.1:n.1014G>T
XM_006719963.2:c.786G>T	XP_006720026.1:p.Arg262Ser
XM_011537474.1:c.1035G>T	XP_011535776.1:p.Arg345Ser
XM_011537475.1:c.849G>T	XP_011535777.1:p.Arg283Ser
XM_011537476.1:c.687G>T	XP_011535778.1:p.Arg229Ser
XM_011537477.1:c.996G>T	XP_011535779.1:p.Arg332Ser
XM_006719963.3:c.831G>T	XP_006720026.2:p.Arg277Ser
XM_011537474.2:c.1080G>T	XP_011535776.2:p.Arg360Ser
XM_011537475.2:c.894G>T	XP_011535777.2:p.Arg298Ser
XM_011537476.2:c.687G>T	XP_011535778.1:p.Arg229Ser
NM_019616.4:c.927G>T MANE Select	NP_062562.1:p.Arg309Ser
NR_051961.2:n.1011G>T
NM_001267554.2:c.741G>T	NP_001254483.1:p.Arg247Ser