Canonical Allele Identifier: CA388785897

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772793C>A (hg19) ; chr13:g.113118479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118479C>A , CM000675.2:g.113118479C>A	GRCh38
NC_000013.10:g.113772793C>A , CM000675.1:g.113772793C>A	GRCh37
NC_000013.9:g.112820794C>A	NCBI36
NG_009258.1:g.681C>A , LRG_548:g.681C>A
NG_009262.1:g.17689C>A , LRG_554:g.17689C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.806C>A MANE Select	ENSP00000329546.4:p.Pro269His
ENST00000346342.7:c.806C>A	ENSP00000329546.3:p.Pro269His
ENST00000375581.3:c.872C>A	ENSP00000364731.3:p.Pro291His
ENST00000541084.5:c.620C>A	ENSP00000442051.2:p.Pro207His
NM_000131.4:c.872C>A , LRG_554t1:c.872C>A	NP_000122.1:p.Pro291His
NM_001267554.1:c.620C>A	NP_001254483.1:p.Pro207His
NM_019616.3:c.806C>A , LRG_554t2:c.806C>A	NP_062562.1:p.Pro269His
NR_051961.1:n.893C>A
XM_006719963.2:c.665C>A	XP_006720026.1:p.Pro222His
XM_011537474.1:c.914C>A	XP_011535776.1:p.Pro305His
XM_011537475.1:c.728C>A	XP_011535777.1:p.Pro243His
XM_011537476.1:c.566C>A	XP_011535778.1:p.Pro189His
XM_011537477.1:c.875C>A	XP_011535779.1:p.Pro292His
XM_006719963.3:c.710C>A	XP_006720026.2:p.Pro237His
XM_011537474.2:c.959C>A	XP_011535776.2:p.Pro320His
XM_011537475.2:c.773C>A	XP_011535777.2:p.Pro258His
XM_011537476.2:c.566C>A	XP_011535778.1:p.Pro189His
NM_019616.4:c.806C>A MANE Select	NP_062562.1:p.Pro269His
NR_051961.2:n.890C>A
NM_001267554.2:c.620C>A	NP_001254483.1:p.Pro207His