Canonical Allele Identifier: CA388786983

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118879G>A , CM000675.2:g.113118879G>A	GRCh38
NC_000013.10:g.113773193G>A , CM000675.1:g.113773193G>A	GRCh37
NC_000013.9:g.112821194G>A	NCBI36
NG_009258.1:g.1081G>A , LRG_548:g.1081G>A
NG_009262.1:g.18089G>A , LRG_554:g.18089G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.1206G>A MANE Select	NP_062562.1:p.Trp402Ter
ENST00000346342.8:c.1206G>A MANE Select	ENSP00000329546.4:p.Trp402Ter
NM_000131.4:c.1272G>A , LRG_554t1:c.1272G>A	NP_000122.1:p.Trp424Ter
NM_001267554.1:c.1020G>A	NP_001254483.1:p.Trp340Ter
NM_001267554.2:c.1020G>A	NP_001254483.1:p.Trp340Ter
NM_019616.3:c.1206G>A , LRG_554t2:c.1206G>A	NP_062562.1:p.Trp402Ter
NR_051961.1:n.1293G>A
NR_051961.2:n.1290G>A
ENST00000346342.7:c.1206G>A	ENSP00000329546.3:p.Trp402Ter
ENST00000375581.3:c.1272G>A	ENSP00000364731.3:p.Trp424Ter
ENST00000541084.5:c.1020G>A	ENSP00000442051.2:p.Trp340Ter
XM_006719963.2:c.1065G>A	XP_006720026.1:p.Trp355Ter
XM_006719963.3:c.1110G>A	XP_006720026.2:p.Trp370Ter
XM_011537474.1:c.1314G>A	XP_011535776.1:p.Trp438Ter
XM_011537474.2:c.1359G>A	XP_011535776.2:p.Trp453Ter
XM_011537475.1:c.1128G>A	XP_011535777.1:p.Trp376Ter
XM_011537475.2:c.1173G>A	XP_011535777.2:p.Trp391Ter
XM_011537476.1:c.966G>A	XP_011535778.1:p.Trp322Ter
XM_011537476.2:c.966G>A	XP_011535778.1:p.Trp322Ter
XM_011537477.1:c.1275G>A	XP_011535779.1:p.Trp425Ter