Canonical Allele Identifier: CA388785878

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772784T>A (hg19) ; chr13:g.113118470T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118470T>A , CM000675.2:g.113118470T>A	GRCh38
NC_000013.10:g.113772784T>A , CM000675.1:g.113772784T>A	GRCh37
NC_000013.9:g.112820785T>A	NCBI36
NG_009258.1:g.672T>A , LRG_548:g.672T>A
NG_009262.1:g.17680T>A , LRG_554:g.17680T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.797T>A MANE Select	ENSP00000329546.4:p.Val266Asp
ENST00000346342.7:c.797T>A	ENSP00000329546.3:p.Val266Asp
ENST00000375581.3:c.863T>A	ENSP00000364731.3:p.Val288Asp
ENST00000541084.5:c.611T>A	ENSP00000442051.2:p.Val204Asp
NM_000131.4:c.863T>A , LRG_554t1:c.863T>A	NP_000122.1:p.Val288Asp
NM_001267554.1:c.611T>A	NP_001254483.1:p.Val204Asp
NM_019616.3:c.797T>A , LRG_554t2:c.797T>A	NP_062562.1:p.Val266Asp
NR_051961.1:n.884T>A
XM_006719963.2:c.656T>A	XP_006720026.1:p.Val219Asp
XM_011537474.1:c.905T>A	XP_011535776.1:p.Val302Asp
XM_011537475.1:c.719T>A	XP_011535777.1:p.Val240Asp
XM_011537476.1:c.557T>A	XP_011535778.1:p.Val186Asp
XM_011537477.1:c.866T>A	XP_011535779.1:p.Val289Asp
XM_006719963.3:c.701T>A	XP_006720026.2:p.Val234Asp
XM_011537474.2:c.950T>A	XP_011535776.2:p.Val317Asp
XM_011537475.2:c.764T>A	XP_011535777.2:p.Val255Asp
XM_011537476.2:c.557T>A	XP_011535778.1:p.Val186Asp
NM_019616.4:c.797T>A MANE Select	NP_062562.1:p.Val266Asp
NR_051961.2:n.881T>A
NM_001267554.2:c.611T>A	NP_001254483.1:p.Val204Asp