Canonical Allele Identifier: CA2120141711

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118435C= , CM000675.2:g.113118435C=	GRCh38
NC_000013.10:g.113772749C= , CM000675.1:g.113772749C=	GRCh37
NC_000013.9:g.112820750C=	NCBI36
NG_009258.1:g.637C= , LRG_548:g.637C=
NG_009262.1:g.17645C= , LRG_554:g.17645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.762C= MANE Select	ENSP00000329546.4:p.His254=
ENST00000346342.7:c.762C=	ENSP00000329546.3:p.His254=
ENST00000375581.3:c.828C=	ENSP00000364731.3:p.His276=
ENST00000541084.5:c.576C=	ENSP00000442051.2:p.His192=
NM_000131.4:c.828C= , LRG_554t1:c.828C=	NP_000122.1:p.His276=
NM_001267554.1:c.576C=	NP_001254483.1:p.His192=
NM_019616.3:c.762C= , LRG_554t2:c.762C=	NP_062562.1:p.His254=
NR_051961.1:n.849C=
XM_006719963.2:c.621C=	XP_006720026.1:p.His207=
XM_011537474.1:c.870C=	XP_011535776.1:p.His290=
XM_011537475.1:c.684C=	XP_011535777.1:p.His228=
XM_011537476.1:c.522C=	XP_011535778.1:p.His174=
XM_011537477.1:c.831C=	XP_011535779.1:p.His277=
XM_006719963.3:c.666C=	XP_006720026.2:p.His222=
XM_011537474.2:c.915C=	XP_011535776.2:p.His305=
XM_011537475.2:c.729C=	XP_011535777.2:p.His243=
XM_011537476.2:c.522C=	XP_011535778.1:p.His174=
NM_019616.4:c.762C= MANE Select	NP_062562.1:p.His254=
NR_051961.2:n.846C=
NM_001267554.2:c.576C=	NP_001254483.1:p.His192=