Canonical Allele Identifier: CA388785815

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772751A>T (hg19) ; chr13:g.113118437A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118437A>T , CM000675.2:g.113118437A>T	GRCh38
NC_000013.10:g.113772751A>T , CM000675.1:g.113772751A>T	GRCh37
NC_000013.9:g.112820752A>T	NCBI36
NG_009258.1:g.639A>T , LRG_548:g.639A>T
NG_009262.1:g.17647A>T , LRG_554:g.17647A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.764A>T MANE Select	ENSP00000329546.4:p.Asp255Val
ENST00000346342.7:c.764A>T	ENSP00000329546.3:p.Asp255Val
ENST00000375581.3:c.830A>T	ENSP00000364731.3:p.Asp277Val
ENST00000541084.5:c.578A>T	ENSP00000442051.2:p.Asp193Val
NM_000131.4:c.830A>T , LRG_554t1:c.830A>T	NP_000122.1:p.Asp277Val
NM_001267554.1:c.578A>T	NP_001254483.1:p.Asp193Val
NM_019616.3:c.764A>T , LRG_554t2:c.764A>T	NP_062562.1:p.Asp255Val
NR_051961.1:n.851A>T
XM_006719963.2:c.623A>T	XP_006720026.1:p.Asp208Val
XM_011537474.1:c.872A>T	XP_011535776.1:p.Asp291Val
XM_011537475.1:c.686A>T	XP_011535777.1:p.Asp229Val
XM_011537476.1:c.524A>T	XP_011535778.1:p.Asp175Val
XM_011537477.1:c.833A>T	XP_011535779.1:p.Asp278Val
XM_006719963.3:c.668A>T	XP_006720026.2:p.Asp223Val
XM_011537474.2:c.917A>T	XP_011535776.2:p.Asp306Val
XM_011537475.2:c.731A>T	XP_011535777.2:p.Asp244Val
XM_011537476.2:c.524A>T	XP_011535778.1:p.Asp175Val
NM_019616.4:c.764A>T MANE Select	NP_062562.1:p.Asp255Val
NR_051961.2:n.848A>T
NM_001267554.2:c.578A>T	NP_001254483.1:p.Asp193Val