Canonical Allele Identifier: CA388782289

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768212A>T (hg19) ; chr13:g.113113898A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113898A>T , CM000675.2:g.113113898A>T	GRCh38
NC_000013.10:g.113768212A>T , CM000675.1:g.113768212A>T	GRCh37
NC_000013.9:g.112816213A>T	NCBI36
NG_009262.1:g.13108A>T , LRG_554:g.13108A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.302A>T MANE Select	ENSP00000329546.4:p.Asp101Val
ENST00000346342.7:c.302A>T	ENSP00000329546.3:p.Asp101Val
ENST00000375581.3:c.368A>T	ENSP00000364731.3:p.Asp123Val
ENST00000444337.1:c.*110A>T	ENSP00000387669.1:n.*110A>T
ENST00000473085.1:n.249A>T
ENST00000479674.1:n.635A>T
ENST00000541084.5:c.116A>T	ENSP00000442051.2:p.Asp39Val
NM_000131.4:c.368A>T , LRG_554t1:c.368A>T	NP_000122.1:p.Asp123Val
NM_001267554.1:c.116A>T	NP_001254483.1:p.Asp39Val
NM_019616.3:c.302A>T , LRG_554t2:c.302A>T	NP_062562.1:p.Asp101Val
NR_051961.1:n.389A>T
XM_006719963.2:c.302A>T	XP_006720026.1:p.Asp101Val
XM_011537474.1:c.302A>T	XP_011535776.1:p.Asp101Val
XM_011537475.1:c.116A>T	XP_011535777.1:p.Asp39Val
XM_011537477.1:c.263A>T	XP_011535779.1:p.Asp88Val
XM_006719963.3:c.347A>T	XP_006720026.2:p.Asp116Val
XM_011537474.2:c.347A>T	XP_011535776.2:p.Asp116Val
XM_011537475.2:c.161A>T	XP_011535777.2:p.Asp54Val
NM_019616.4:c.302A>T MANE Select	NP_062562.1:p.Asp101Val
NR_051961.2:n.386A>T
NM_001267554.2:c.116A>T	NP_001254483.1:p.Asp39Val