Canonical Allele Identifier: CA2120142771

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118839A= , CM000675.2:g.113118839A=	GRCh38
NC_000013.10:g.113773153A= , CM000675.1:g.113773153A=	GRCh37
NC_000013.9:g.112821154A=	NCBI36
NG_009258.1:g.1041A= , LRG_548:g.1041A=
NG_009262.1:g.18049A= , LRG_554:g.18049A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1166A= MANE Select	ENSP00000329546.4:p.His389=
ENST00000346342.7:c.1166A=	ENSP00000329546.3:p.His389=
ENST00000375581.3:c.1232A=	ENSP00000364731.3:p.His411=
ENST00000541084.5:c.980A=	ENSP00000442051.2:p.His327=
NM_000131.4:c.1232A= , LRG_554t1:c.1232A=	NP_000122.1:p.His411=
NM_001267554.1:c.980A=	NP_001254483.1:p.His327=
NM_019616.3:c.1166A= , LRG_554t2:c.1166A=	NP_062562.1:p.His389=
NR_051961.1:n.1253A=
XM_006719963.2:c.1025A=	XP_006720026.1:p.His342=
XM_011537474.1:c.1274A=	XP_011535776.1:p.His425=
XM_011537475.1:c.1088A=	XP_011535777.1:p.His363=
XM_011537476.1:c.926A=	XP_011535778.1:p.His309=
XM_011537477.1:c.1235A=	XP_011535779.1:p.His412=
XM_006719963.3:c.1070A=	XP_006720026.2:p.His357=
XM_011537474.2:c.1319A=	XP_011535776.2:p.His440=
XM_011537475.2:c.1133A=	XP_011535777.2:p.His378=
XM_011537476.2:c.926A=	XP_011535778.1:p.His309=
NM_019616.4:c.1166A= MANE Select	NP_062562.1:p.His389=
NR_051961.2:n.1250A=
NM_001267554.2:c.980A=	NP_001254483.1:p.His327=