Canonical Allele Identifier: CA388786295

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772997T>A (hg19) ; chr13:g.113118683T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118683T>A , CM000675.2:g.113118683T>A	GRCh38
NC_000013.10:g.113772997T>A , CM000675.1:g.113772997T>A	GRCh37
NC_000013.9:g.112820998T>A	NCBI36
NG_009258.1:g.885T>A , LRG_548:g.885T>A
NG_009262.1:g.17893T>A , LRG_554:g.17893T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1010T>A MANE Select	ENSP00000329546.4:p.Val337Asp
ENST00000346342.7:c.1010T>A	ENSP00000329546.3:p.Val337Asp
ENST00000375581.3:c.1076T>A	ENSP00000364731.3:p.Val359Asp
ENST00000541084.5:c.824T>A	ENSP00000442051.2:p.Val275Asp
NM_000131.4:c.1076T>A , LRG_554t1:c.1076T>A	NP_000122.1:p.Val359Asp
NM_001267554.1:c.824T>A	NP_001254483.1:p.Val275Asp
NM_019616.3:c.1010T>A , LRG_554t2:c.1010T>A	NP_062562.1:p.Val337Asp
NR_051961.1:n.1097T>A
XM_006719963.2:c.869T>A	XP_006720026.1:p.Val290Asp
XM_011537474.1:c.1118T>A	XP_011535776.1:p.Val373Asp
XM_011537475.1:c.932T>A	XP_011535777.1:p.Val311Asp
XM_011537476.1:c.770T>A	XP_011535778.1:p.Val257Asp
XM_011537477.1:c.1079T>A	XP_011535779.1:p.Val360Asp
XM_006719963.3:c.914T>A	XP_006720026.2:p.Val305Asp
XM_011537474.2:c.1163T>A	XP_011535776.2:p.Val388Asp
XM_011537475.2:c.977T>A	XP_011535777.2:p.Val326Asp
XM_011537476.2:c.770T>A	XP_011535778.1:p.Val257Asp
NM_019616.4:c.1010T>A MANE Select	NP_062562.1:p.Val337Asp
NR_051961.2:n.1094T>A
NM_001267554.2:c.824T>A	NP_001254483.1:p.Val275Asp