Canonical Allele Identifier: CA1206135851

Gene: F5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169529791C= , CM000663.2:g.169529791C=	GRCh38
NC_000001.10:g.169499029C= , CM000663.1:g.169499029C=	GRCh37
NC_000001.9:g.167765653C=	NCBI36
NG_011806.1:g.61741G= , LRG_553:g.61741G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.5236G= MANE Select	ENSP00000356771.3:p.Gly1746=
ENST00000367796.3:c.5251G=	ENSP00000356770.3:p.Gly1751=
ENST00000367797.7:c.5236G=	ENSP00000356771.3:p.Gly1746=
NM_000130.4:c.5236G= , LRG_553t1:c.5236G=	NP_000121.2:p.Gly1746=
XM_017000660.2:c.4825G=	XP_016856149.1:p.Gly1609=
NM_000130.5:c.5236G= MANE Select	NP_000121.2:p.Gly1746=