Canonical Allele Identifier: CA388786414

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773056G>A (hg19) ; chr13:g.113118742G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118742G>A , CM000675.2:g.113118742G>A	GRCh38
NC_000013.10:g.113773056G>A , CM000675.1:g.113773056G>A	GRCh37
NC_000013.9:g.112821057G>A	NCBI36
NG_009258.1:g.944G>A , LRG_548:g.944G>A
NG_009262.1:g.17952G>A , LRG_554:g.17952G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1069G>A MANE Select	ENSP00000329546.4:p.Asp357Asn
ENST00000346342.7:c.1069G>A	ENSP00000329546.3:p.Asp357Asn
ENST00000375581.3:c.1135G>A	ENSP00000364731.3:p.Asp379Asn
ENST00000541084.5:c.883G>A	ENSP00000442051.2:p.Asp295Asn
NM_000131.4:c.1135G>A , LRG_554t1:c.1135G>A	NP_000122.1:p.Asp379Asn
NM_001267554.1:c.883G>A	NP_001254483.1:p.Asp295Asn
NM_019616.3:c.1069G>A , LRG_554t2:c.1069G>A	NP_062562.1:p.Asp357Asn
NR_051961.1:n.1156G>A
XM_006719963.2:c.928G>A	XP_006720026.1:p.Asp310Asn
XM_011537474.1:c.1177G>A	XP_011535776.1:p.Asp393Asn
XM_011537475.1:c.991G>A	XP_011535777.1:p.Asp331Asn
XM_011537476.1:c.829G>A	XP_011535778.1:p.Asp277Asn
XM_011537477.1:c.1138G>A	XP_011535779.1:p.Asp380Asn
XM_006719963.3:c.973G>A	XP_006720026.2:p.Asp325Asn
XM_011537474.2:c.1222G>A	XP_011535776.2:p.Asp408Asn
XM_011537475.2:c.1036G>A	XP_011535777.2:p.Asp346Asn
XM_011537476.2:c.829G>A	XP_011535778.1:p.Asp277Asn
NM_019616.4:c.1069G>A MANE Select	NP_062562.1:p.Asp357Asn
NR_051961.2:n.1153G>A
NM_001267554.2:c.883G>A	NP_001254483.1:p.Asp295Asn