Canonical Allele Identifier: CA388784983

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113116841G>A , CM000675.2:g.113116841G>A	GRCh38
NC_000013.10:g.113771155G>A , CM000675.1:g.113771155G>A	GRCh37
NC_000013.9:g.112819156G>A	NCBI36
NG_009262.1:g.16051G>A , LRG_554:g.16051G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.581G>A MANE Select	NP_062562.1:p.Gly194Asp
ENST00000346342.8:c.581G>A MANE Select	ENSP00000329546.4:p.Gly194Asp
NM_000131.4:c.647G>A , LRG_554t1:c.647G>A	NP_000122.1:p.Gly216Asp
NM_001267554.1:c.395G>A	NP_001254483.1:p.Gly132Asp
NM_001267554.2:c.395G>A	NP_001254483.1:p.Gly132Asp
NM_019616.3:c.581G>A , LRG_554t2:c.581G>A	NP_062562.1:p.Gly194Asp
NR_051961.1:n.668G>A
NR_051961.2:n.665G>A
ENST00000346342.7:c.581G>A	ENSP00000329546.3:p.Gly194Asp
ENST00000375581.3:c.647G>A	ENSP00000364731.3:p.Gly216Asp
ENST00000541084.5:c.395G>A	ENSP00000442051.2:p.Gly132Asp
XM_006719963.2:c.440G>A	XP_006720026.1:p.Gly147Asp
XM_006719963.3:c.485G>A	XP_006720026.2:p.Gly162Asp
XM_011537474.1:c.689G>A	XP_011535776.1:p.Gly230Asp
XM_011537474.2:c.734G>A	XP_011535776.2:p.Gly245Asp
XM_011537475.1:c.503G>A	XP_011535777.1:p.Gly168Asp
XM_011537475.2:c.548G>A	XP_011535777.2:p.Gly183Asp
XM_011537476.1:c.341G>A	XP_011535778.1:p.Gly114Asp
XM_011537476.2:c.341G>A	XP_011535778.1:p.Gly114Asp
XM_011537477.1:c.650G>A	XP_011535779.1:p.Gly217Asp