Canonical Allele Identifier: CA1206132623

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169542027C= , CM000663.2:g.169542027C=	GRCh38
NC_000001.10:g.169511265C= , CM000663.1:g.169511265C=	GRCh37
NC_000001.9:g.167777889C=	NCBI36
NG_011806.1:g.49505G= , LRG_553:g.49505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3063G= MANE Select	ENSP00000356771.3:p.Lys1021=
ENST00000367796.3:c.3078G=	ENSP00000356770.3:p.Lys1026=
ENST00000367797.7:c.3063G=	ENSP00000356771.3:p.Lys1021=
NM_000130.4:c.3063G= , LRG_553t1:c.3063G=	NP_000121.2:p.Lys1021=
XM_017000660.2:c.2652G=	XP_016856149.1:p.Lys884=
NM_000130.5:c.3063G= MANE Select	NP_000121.2:p.Lys1021=