Canonical Allele Identifier: CA388786241

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772967A>T (hg19) ; chr13:g.113118653A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118653A>T , CM000675.2:g.113118653A>T	GRCh38
NC_000013.10:g.113772967A>T , CM000675.1:g.113772967A>T	GRCh37
NC_000013.9:g.112820968A>T	NCBI36
NG_009258.1:g.855A>T , LRG_548:g.855A>T
NG_009262.1:g.17863A>T , LRG_554:g.17863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.980A>T MANE Select	ENSP00000329546.4:p.Asp327Val
ENST00000346342.7:c.980A>T	ENSP00000329546.3:p.Asp327Val
ENST00000375581.3:c.1046A>T	ENSP00000364731.3:p.Asp349Val
ENST00000541084.5:c.794A>T	ENSP00000442051.2:p.Asp265Val
NM_000131.4:c.1046A>T , LRG_554t1:c.1046A>T	NP_000122.1:p.Asp349Val
NM_001267554.1:c.794A>T	NP_001254483.1:p.Asp265Val
NM_019616.3:c.980A>T , LRG_554t2:c.980A>T	NP_062562.1:p.Asp327Val
NR_051961.1:n.1067A>T
XM_006719963.2:c.839A>T	XP_006720026.1:p.Asp280Val
XM_011537474.1:c.1088A>T	XP_011535776.1:p.Asp363Val
XM_011537475.1:c.902A>T	XP_011535777.1:p.Asp301Val
XM_011537476.1:c.740A>T	XP_011535778.1:p.Asp247Val
XM_011537477.1:c.1049A>T	XP_011535779.1:p.Asp350Val
XM_006719963.3:c.884A>T	XP_006720026.2:p.Asp295Val
XM_011537474.2:c.1133A>T	XP_011535776.2:p.Asp378Val
XM_011537475.2:c.947A>T	XP_011535777.2:p.Asp316Val
XM_011537476.2:c.740A>T	XP_011535778.1:p.Asp247Val
NM_019616.4:c.980A>T MANE Select	NP_062562.1:p.Asp327Val
NR_051961.2:n.1064A>T
NM_001267554.2:c.794A>T	NP_001254483.1:p.Asp265Val