Canonical Allele Identifier: CA388786259

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772978A>G (hg19) ; chr13:g.113118664A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118664A>G , CM000675.2:g.113118664A>G	GRCh38
NC_000013.10:g.113772978A>G , CM000675.1:g.113772978A>G	GRCh37
NC_000013.9:g.112820979A>G	NCBI36
NG_009258.1:g.866A>G , LRG_548:g.866A>G
NG_009262.1:g.17874A>G , LRG_554:g.17874A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.991A>G MANE Select	ENSP00000329546.4:p.Thr331Ala
ENST00000346342.7:c.991A>G	ENSP00000329546.3:p.Thr331Ala
ENST00000375581.3:c.1057A>G	ENSP00000364731.3:p.Thr353Ala
ENST00000541084.5:c.805A>G	ENSP00000442051.2:p.Thr269Ala
NM_000131.4:c.1057A>G , LRG_554t1:c.1057A>G	NP_000122.1:p.Thr353Ala
NM_001267554.1:c.805A>G	NP_001254483.1:p.Thr269Ala
NM_019616.3:c.991A>G , LRG_554t2:c.991A>G	NP_062562.1:p.Thr331Ala
NR_051961.1:n.1078A>G
XM_006719963.2:c.850A>G	XP_006720026.1:p.Thr284Ala
XM_011537474.1:c.1099A>G	XP_011535776.1:p.Thr367Ala
XM_011537475.1:c.913A>G	XP_011535777.1:p.Thr305Ala
XM_011537476.1:c.751A>G	XP_011535778.1:p.Thr251Ala
XM_011537477.1:c.1060A>G	XP_011535779.1:p.Thr354Ala
XM_006719963.3:c.895A>G	XP_006720026.2:p.Thr299Ala
XM_011537474.2:c.1144A>G	XP_011535776.2:p.Thr382Ala
XM_011537475.2:c.958A>G	XP_011535777.2:p.Thr320Ala
XM_011537476.2:c.751A>G	XP_011535778.1:p.Thr251Ala
NM_019616.4:c.991A>G MANE Select	NP_062562.1:p.Thr331Ala
NR_051961.2:n.1075A>G
NM_001267554.2:c.805A>G	NP_001254483.1:p.Thr269Ala