Canonical Allele Identifier: CA2120141959

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118507C= , CM000675.2:g.113118507C=	GRCh38
NC_000013.10:g.113772821C= , CM000675.1:g.113772821C=	GRCh37
NC_000013.9:g.112820822C=	NCBI36
NG_009258.1:g.709C= , LRG_548:g.709C=
NG_009262.1:g.17717C= , LRG_554:g.17717C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.834C= MANE Select	ENSP00000329546.4:p.Asn278=
ENST00000346342.7:c.834C=	ENSP00000329546.3:p.Asn278=
ENST00000375581.3:c.900C=	ENSP00000364731.3:p.Asn300=
ENST00000541084.5:c.648C=	ENSP00000442051.2:p.Asn216=
NM_000131.4:c.900C= , LRG_554t1:c.900C=	NP_000122.1:p.Asn300=
NM_001267554.1:c.648C=	NP_001254483.1:p.Asn216=
NM_019616.3:c.834C= , LRG_554t2:c.834C=	NP_062562.1:p.Asn278=
NR_051961.1:n.921C=
XM_006719963.2:c.693C=	XP_006720026.1:p.Asn231=
XM_011537474.1:c.942C=	XP_011535776.1:p.Asn314=
XM_011537475.1:c.756C=	XP_011535777.1:p.Asn252=
XM_011537476.1:c.594C=	XP_011535778.1:p.Asn198=
XM_011537477.1:c.903C=	XP_011535779.1:p.Asn301=
XM_006719963.3:c.738C=	XP_006720026.2:p.Asn246=
XM_011537474.2:c.987C=	XP_011535776.2:p.Asn329=
XM_011537475.2:c.801C=	XP_011535777.2:p.Asn267=
XM_011537476.2:c.594C=	XP_011535778.1:p.Asn198=
NM_019616.4:c.834C= MANE Select	NP_062562.1:p.Asn278=
NR_051961.2:n.918C=
NM_001267554.2:c.648C=	NP_001254483.1:p.Asn216=