Canonical Allele Identifier: CA388786002

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772848C>A (hg19) ; chr13:g.113118534C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118534C>A , CM000675.2:g.113118534C>A	GRCh38
NC_000013.10:g.113772848C>A , CM000675.1:g.113772848C>A	GRCh37
NC_000013.9:g.112820849C>A	NCBI36
NG_009258.1:g.736C>A , LRG_548:g.736C>A
NG_009262.1:g.17744C>A , LRG_554:g.17744C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.861C>A MANE Select	ENSP00000329546.4:p.His287Gln
ENST00000346342.7:c.861C>A	ENSP00000329546.3:p.His287Gln
ENST00000375581.3:c.927C>A	ENSP00000364731.3:p.His309Gln
ENST00000541084.5:c.675C>A	ENSP00000442051.2:p.His225Gln
NM_000131.4:c.927C>A , LRG_554t1:c.927C>A	NP_000122.1:p.His309Gln
NM_001267554.1:c.675C>A	NP_001254483.1:p.His225Gln
NM_019616.3:c.861C>A , LRG_554t2:c.861C>A	NP_062562.1:p.His287Gln
NR_051961.1:n.948C>A
XM_006719963.2:c.720C>A	XP_006720026.1:p.His240Gln
XM_011537474.1:c.969C>A	XP_011535776.1:p.His323Gln
XM_011537475.1:c.783C>A	XP_011535777.1:p.His261Gln
XM_011537476.1:c.621C>A	XP_011535778.1:p.His207Gln
XM_011537477.1:c.930C>A	XP_011535779.1:p.His310Gln
XM_006719963.3:c.765C>A	XP_006720026.2:p.His255Gln
XM_011537474.2:c.1014C>A	XP_011535776.2:p.His338Gln
XM_011537475.2:c.828C>A	XP_011535777.2:p.His276Gln
XM_011537476.2:c.621C>A	XP_011535778.1:p.His207Gln
NM_019616.4:c.861C>A MANE Select	NP_062562.1:p.His287Gln
NR_051961.2:n.945C>A
NM_001267554.2:c.675C>A	NP_001254483.1:p.His225Gln