Canonical Allele Identifier: CA1206148958

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169554921C= , CM000663.2:g.169554921C=	GRCh38
NC_000001.10:g.169524159C= , CM000663.1:g.169524159C=	GRCh37
NC_000001.9:g.167790783C=	NCBI36
NG_011806.1:g.36611G= , LRG_553:g.36611G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1118+261G= MANE Select	ENSP00000356771.3:n.1118+261G=
ENST00000367796.3:c.1118+261G=	ENSP00000356770.3:n.1118+261G=
ENST00000367797.7:c.1118+261G=	ENSP00000356771.3:n.1118+261G=
NM_000130.4:c.1118+261G= , LRG_553t1:c.1118+261G=	NP_000121.2:n.1118+261G=
XM_017000660.2:c.707+261G=	XP_016856149.1:n.707+261G=
NM_000130.5:c.1118+261G= MANE Select	NP_000121.2:n.1118+261G=