Canonical Allele Identifier: CA388785807

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772747C>A (hg19) ; chr13:g.113118433C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118433C>A , CM000675.2:g.113118433C>A	GRCh38
NC_000013.10:g.113772747C>A , CM000675.1:g.113772747C>A	GRCh37
NC_000013.9:g.112820748C>A	NCBI36
NG_009258.1:g.635C>A , LRG_548:g.635C>A
NG_009262.1:g.17643C>A , LRG_554:g.17643C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.760C>A MANE Select	ENSP00000329546.4:p.His254Asn
ENST00000346342.7:c.760C>A	ENSP00000329546.3:p.His254Asn
ENST00000375581.3:c.826C>A	ENSP00000364731.3:p.His276Asn
ENST00000541084.5:c.574C>A	ENSP00000442051.2:p.His192Asn
NM_000131.4:c.826C>A , LRG_554t1:c.826C>A	NP_000122.1:p.His276Asn
NM_001267554.1:c.574C>A	NP_001254483.1:p.His192Asn
NM_019616.3:c.760C>A , LRG_554t2:c.760C>A	NP_062562.1:p.His254Asn
NR_051961.1:n.847C>A
XM_006719963.2:c.619C>A	XP_006720026.1:p.His207Asn
XM_011537474.1:c.868C>A	XP_011535776.1:p.His290Asn
XM_011537475.1:c.682C>A	XP_011535777.1:p.His228Asn
XM_011537476.1:c.520C>A	XP_011535778.1:p.His174Asn
XM_011537477.1:c.829C>A	XP_011535779.1:p.His277Asn
XM_006719963.3:c.664C>A	XP_006720026.2:p.His222Asn
XM_011537474.2:c.913C>A	XP_011535776.2:p.His305Asn
XM_011537475.2:c.727C>A	XP_011535777.2:p.His243Asn
XM_011537476.2:c.520C>A	XP_011535778.1:p.His174Asn
NM_019616.4:c.760C>A MANE Select	NP_062562.1:p.His254Asn
NR_051961.2:n.844C>A
NM_001267554.2:c.574C>A	NP_001254483.1:p.His192Asn