Canonical Allele Identifier: CA343128696

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169521901G>A (hg19) ; chr1:g.169552663G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169552663G>A , CM000663.2:g.169552663G>A	GRCh38
NC_000001.10:g.169521901G>A , CM000663.1:g.169521901G>A	GRCh37
NC_000001.9:g.167788525G>A	NCBI36
NG_011806.1:g.38869C>T , LRG_553:g.38869C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.1190C>T MANE Select	ENSP00000356771.3:p.Thr397Ile
ENST00000367796.3:c.1190C>T	ENSP00000356770.3:p.Thr397Ile
ENST00000367797.7:c.1190C>T	ENSP00000356771.3:p.Thr397Ile
NM_000130.4:c.1190C>T , LRG_553t1:c.1190C>T	NP_000121.2:p.Thr397Ile
XM_017000660.2:c.779C>T	XP_016856149.1:p.Thr260Ile
NM_000130.5:c.1190C>T MANE Select	NP_000121.2:p.Thr397Ile