Canonical Allele Identifier: CA388785896

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772792C>G (hg19) ; chr13:g.113118478C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118478C>G , CM000675.2:g.113118478C>G	GRCh38
NC_000013.10:g.113772792C>G , CM000675.1:g.113772792C>G	GRCh37
NC_000013.9:g.112820793C>G	NCBI36
NG_009258.1:g.680C>G , LRG_548:g.680C>G
NG_009262.1:g.17688C>G , LRG_554:g.17688C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.805C>G MANE Select	ENSP00000329546.4:p.Pro269Ala
ENST00000346342.7:c.805C>G	ENSP00000329546.3:p.Pro269Ala
ENST00000375581.3:c.871C>G	ENSP00000364731.3:p.Pro291Ala
ENST00000541084.5:c.619C>G	ENSP00000442051.2:p.Pro207Ala
NM_000131.4:c.871C>G , LRG_554t1:c.871C>G	NP_000122.1:p.Pro291Ala
NM_001267554.1:c.619C>G	NP_001254483.1:p.Pro207Ala
NM_019616.3:c.805C>G , LRG_554t2:c.805C>G	NP_062562.1:p.Pro269Ala
NR_051961.1:n.892C>G
XM_006719963.2:c.664C>G	XP_006720026.1:p.Pro222Ala
XM_011537474.1:c.913C>G	XP_011535776.1:p.Pro305Ala
XM_011537475.1:c.727C>G	XP_011535777.1:p.Pro243Ala
XM_011537476.1:c.565C>G	XP_011535778.1:p.Pro189Ala
XM_011537477.1:c.874C>G	XP_011535779.1:p.Pro292Ala
XM_006719963.3:c.709C>G	XP_006720026.2:p.Pro237Ala
XM_011537474.2:c.958C>G	XP_011535776.2:p.Pro320Ala
XM_011537475.2:c.772C>G	XP_011535777.2:p.Pro258Ala
XM_011537476.2:c.565C>G	XP_011535778.1:p.Pro189Ala
NM_019616.4:c.805C>G MANE Select	NP_062562.1:p.Pro269Ala
NR_051961.2:n.889C>G
NM_001267554.2:c.619C>G	NP_001254483.1:p.Pro207Ala