Canonical Allele Identifier: CA388785969

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772829T>A (hg19) ; chr13:g.113118515T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118515T>A , CM000675.2:g.113118515T>A	GRCh38
NC_000013.10:g.113772829T>A , CM000675.1:g.113772829T>A	GRCh37
NC_000013.9:g.112820830T>A	NCBI36
NG_009258.1:g.717T>A , LRG_548:g.717T>A
NG_009262.1:g.17725T>A , LRG_554:g.17725T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.842T>A MANE Select	ENSP00000329546.4:p.Ile281Asn
ENST00000346342.7:c.842T>A	ENSP00000329546.3:p.Ile281Asn
ENST00000375581.3:c.908T>A	ENSP00000364731.3:p.Ile303Asn
ENST00000541084.5:c.656T>A	ENSP00000442051.2:p.Ile219Asn
NM_000131.4:c.908T>A , LRG_554t1:c.908T>A	NP_000122.1:p.Ile303Asn
NM_001267554.1:c.656T>A	NP_001254483.1:p.Ile219Asn
NM_019616.3:c.842T>A , LRG_554t2:c.842T>A	NP_062562.1:p.Ile281Asn
NR_051961.1:n.929T>A
XM_006719963.2:c.701T>A	XP_006720026.1:p.Ile234Asn
XM_011537474.1:c.950T>A	XP_011535776.1:p.Ile317Asn
XM_011537475.1:c.764T>A	XP_011535777.1:p.Ile255Asn
XM_011537476.1:c.602T>A	XP_011535778.1:p.Ile201Asn
XM_011537477.1:c.911T>A	XP_011535779.1:p.Ile304Asn
XM_006719963.3:c.746T>A	XP_006720026.2:p.Ile249Asn
XM_011537474.2:c.995T>A	XP_011535776.2:p.Ile332Asn
XM_011537475.2:c.809T>A	XP_011535777.2:p.Ile270Asn
XM_011537476.2:c.602T>A	XP_011535778.1:p.Ile201Asn
NM_019616.4:c.842T>A MANE Select	NP_062562.1:p.Ile281Asn
NR_051961.2:n.926T>A
NM_001267554.2:c.656T>A	NP_001254483.1:p.Ile219Asn