Canonical Allele Identifier: CA388787124

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118945G>A , CM000675.2:g.113118945G>A	GRCh38
NC_000013.10:g.113773259G>A , CM000675.1:g.113773259G>A	GRCh37
NC_000013.9:g.112821260G>A	NCBI36
NG_009258.1:g.1147G>A , LRG_548:g.1147G>A
NG_009262.1:g.18155G>A , LRG_554:g.18155G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.1272G>A MANE Select	NP_062562.1:p.Trp424Ter
ENST00000346342.8:c.1272G>A MANE Select	ENSP00000329546.4:p.Trp424Ter
NM_000131.4:c.1338G>A , LRG_554t1:c.1338G>A	NP_000122.1:p.Trp446Ter
NM_001267554.1:c.1086G>A	NP_001254483.1:p.Trp362Ter
NM_001267554.2:c.1086G>A	NP_001254483.1:p.Trp362Ter
NM_019616.3:c.1272G>A , LRG_554t2:c.1272G>A	NP_062562.1:p.Trp424Ter
NR_051961.1:n.1359G>A
NR_051961.2:n.1356G>A
ENST00000346342.7:c.1272G>A	ENSP00000329546.3:p.Trp424Ter
ENST00000375581.3:c.1338G>A	ENSP00000364731.3:p.Trp446Ter
ENST00000541084.5:c.1086G>A	ENSP00000442051.2:p.Trp362Ter
XM_006719963.2:c.1131G>A	XP_006720026.1:p.Trp377Ter
XM_006719963.3:c.1176G>A	XP_006720026.2:p.Trp392Ter
XM_011537474.1:c.1380G>A	XP_011535776.1:p.Trp460Ter
XM_011537474.2:c.1425G>A	XP_011535776.2:p.Trp475Ter
XM_011537475.1:c.1194G>A	XP_011535777.1:p.Trp398Ter
XM_011537475.2:c.1239G>A	XP_011535777.2:p.Trp413Ter
XM_011537476.1:c.1032G>A	XP_011535778.1:p.Trp344Ter
XM_011537476.2:c.1032G>A	XP_011535778.1:p.Trp344Ter
XM_011537477.1:c.1341G>A	XP_011535779.1:p.Trp447Ter