Canonical Allele Identifier: CA2120143151

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118994G= , CM000675.2:g.113118994G=	GRCh38
NC_000013.10:g.113773308G= , CM000675.1:g.113773308G=	GRCh37
NC_000013.9:g.112821309G=	NCBI36
NG_009258.1:g.1196G= , LRG_548:g.1196G=
NG_009262.1:g.18204G= , LRG_554:g.18204G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1321G= MANE Select	ENSP00000329546.4:p.Ala441=
ENST00000346342.7:c.1321G=	ENSP00000329546.3:p.Ala441=
ENST00000375581.3:c.1387G=	ENSP00000364731.3:p.Ala463=
ENST00000541084.5:c.1135G=	ENSP00000442051.2:p.Ala379=
NM_000131.4:c.1387G= , LRG_554t1:c.1387G=	NP_000122.1:p.Ala463=
NM_001267554.1:c.1135G=	NP_001254483.1:p.Ala379=
NM_019616.3:c.1321G= , LRG_554t2:c.1321G=	NP_062562.1:p.Ala441=
NR_051961.1:n.1408G=
XM_006719963.2:c.1180G=	XP_006720026.1:p.Ala394=
XM_011537474.1:c.1429G=	XP_011535776.1:p.Ala477=
XM_011537475.1:c.1243G=	XP_011535777.1:p.Ala415=
XM_011537476.1:c.1081G=	XP_011535778.1:p.Ala361=
XM_011537477.1:c.1390G=	XP_011535779.1:p.Ala464=
XM_006719963.3:c.1225G=	XP_006720026.2:p.Ala409=
XM_011537474.2:c.1474G=	XP_011535776.2:p.Ala492=
XM_011537475.2:c.1288G=	XP_011535777.2:p.Ala430=
XM_011537476.2:c.1081G=	XP_011535778.1:p.Ala361=
NM_019616.4:c.1321G= MANE Select	NP_062562.1:p.Ala441=
NR_051961.2:n.1405G=
NM_001267554.2:c.1135G=	NP_001254483.1:p.Ala379=