Canonical Allele Identifier: CA2120143156

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119000T= , CM000675.2:g.113119000T=	GRCh38
NC_000013.10:g.113773314T= , CM000675.1:g.113773314T=	GRCh37
NC_000013.9:g.112821315T=	NCBI36
NG_009258.1:g.1202T= , LRG_548:g.1202T=
NG_009262.1:g.18210T= , LRG_554:g.18210T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1327T= MANE Select	ENSP00000329546.4:p.Phe443=
ENST00000346342.7:c.1327T=	ENSP00000329546.3:p.Phe443=
ENST00000375581.3:c.1393T=	ENSP00000364731.3:p.Phe465=
ENST00000541084.5:c.1141T=	ENSP00000442051.2:p.Phe381=
NM_000131.4:c.1393T= , LRG_554t1:c.1393T=	NP_000122.1:p.Phe465=
NM_001267554.1:c.1141T=	NP_001254483.1:p.Phe381=
NM_019616.3:c.1327T= , LRG_554t2:c.1327T=	NP_062562.1:p.Phe443=
NR_051961.1:n.1414T=
XM_006719963.2:c.1186T=	XP_006720026.1:p.Phe396=
XM_011537474.1:c.1435T=	XP_011535776.1:p.Phe479=
XM_011537475.1:c.1249T=	XP_011535777.1:p.Phe417=
XM_011537476.1:c.1087T=	XP_011535778.1:p.Phe363=
XM_011537477.1:c.1396T=	XP_011535779.1:p.Phe466=
XM_006719963.3:c.1231T=	XP_006720026.2:p.Phe411=
XM_011537474.2:c.1480T=	XP_011535776.2:p.Phe494=
XM_011537475.2:c.1294T=	XP_011535777.2:p.Phe432=
XM_011537476.2:c.1087T=	XP_011535778.1:p.Phe363=
NM_019616.4:c.1327T= MANE Select	NP_062562.1:p.Phe443=
NR_051961.2:n.1411T=
NM_001267554.2:c.1141T=	NP_001254483.1:p.Phe381=