Canonical Allele Identifier: CA2120141704

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118433C= , CM000675.2:g.113118433C=	GRCh38
NC_000013.10:g.113772747C= , CM000675.1:g.113772747C=	GRCh37
NC_000013.9:g.112820748C=	NCBI36
NG_009258.1:g.635C= , LRG_548:g.635C=
NG_009262.1:g.17643C= , LRG_554:g.17643C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.760C= MANE Select	ENSP00000329546.4:p.His254=
ENST00000346342.7:c.760C=	ENSP00000329546.3:p.His254=
ENST00000375581.3:c.826C=	ENSP00000364731.3:p.His276=
ENST00000541084.5:c.574C=	ENSP00000442051.2:p.His192=
NM_000131.4:c.826C= , LRG_554t1:c.826C=	NP_000122.1:p.His276=
NM_001267554.1:c.574C=	NP_001254483.1:p.His192=
NM_019616.3:c.760C= , LRG_554t2:c.760C=	NP_062562.1:p.His254=
NR_051961.1:n.847C=
XM_006719963.2:c.619C=	XP_006720026.1:p.His207=
XM_011537474.1:c.868C=	XP_011535776.1:p.His290=
XM_011537475.1:c.682C=	XP_011535777.1:p.His228=
XM_011537476.1:c.520C=	XP_011535778.1:p.His174=
XM_011537477.1:c.829C=	XP_011535779.1:p.His277=
XM_006719963.3:c.664C=	XP_006720026.2:p.His222=
XM_011537474.2:c.913C=	XP_011535776.2:p.His305=
XM_011537475.2:c.727C=	XP_011535777.2:p.His243=
XM_011537476.2:c.520C=	XP_011535778.1:p.His174=
NM_019616.4:c.760C= MANE Select	NP_062562.1:p.His254=
NR_051961.2:n.844C=
NM_001267554.2:c.574C=	NP_001254483.1:p.His192=