Canonical Allele Identifier: CA388785889

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772789A>T (hg19) ; chr13:g.113118475A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118475A>T , CM000675.2:g.113118475A>T	GRCh38
NC_000013.10:g.113772789A>T , CM000675.1:g.113772789A>T	GRCh37
NC_000013.9:g.112820790A>T	NCBI36
NG_009258.1:g.677A>T , LRG_548:g.677A>T
NG_009262.1:g.17685A>T , LRG_554:g.17685A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.802A>T MANE Select	ENSP00000329546.4:p.Ile268Phe
ENST00000346342.7:c.802A>T	ENSP00000329546.3:p.Ile268Phe
ENST00000375581.3:c.868A>T	ENSP00000364731.3:p.Ile290Phe
ENST00000541084.5:c.616A>T	ENSP00000442051.2:p.Ile206Phe
NM_000131.4:c.868A>T , LRG_554t1:c.868A>T	NP_000122.1:p.Ile290Phe
NM_001267554.1:c.616A>T	NP_001254483.1:p.Ile206Phe
NM_019616.3:c.802A>T , LRG_554t2:c.802A>T	NP_062562.1:p.Ile268Phe
NR_051961.1:n.889A>T
XM_006719963.2:c.661A>T	XP_006720026.1:p.Ile221Phe
XM_011537474.1:c.910A>T	XP_011535776.1:p.Ile304Phe
XM_011537475.1:c.724A>T	XP_011535777.1:p.Ile242Phe
XM_011537476.1:c.562A>T	XP_011535778.1:p.Ile188Phe
XM_011537477.1:c.871A>T	XP_011535779.1:p.Ile291Phe
XM_006719963.3:c.706A>T	XP_006720026.2:p.Ile236Phe
XM_011537474.2:c.955A>T	XP_011535776.2:p.Ile319Phe
XM_011537475.2:c.769A>T	XP_011535777.2:p.Ile257Phe
XM_011537476.2:c.562A>T	XP_011535778.1:p.Ile188Phe
NM_019616.4:c.802A>T MANE Select	NP_062562.1:p.Ile268Phe
NR_051961.2:n.886A>T
NM_001267554.2:c.616A>T	NP_001254483.1:p.Ile206Phe