Canonical Allele Identifier: CA343117937
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169541663C>A , CM000663.2:g.169541663C>A GRCh38
NC_000001.10:g.169510901C>A , CM000663.1:g.169510901C>A GRCh37
NC_000001.9:g.167777525C>A NCBI36
NG_011806.1:g.49869G>T , LRG_553:g.49869G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.3427G>T MANE Select ENSP00000356771.3:p.Asp1143Tyr
ENST00000367796.3:c.3442G>T ENSP00000356770.3:p.Asp1148Tyr
ENST00000367797.7:c.3427G>T ENSP00000356771.3:p.Asp1143Tyr
NM_000130.4:c.3427G>T , LRG_553t1:c.3427G>T NP_000121.2:p.Asp1143Tyr
XM_017000660.2:c.3016G>T XP_016856149.1:p.Asp1006Tyr
NM_000130.5:c.3427G>T MANE Select NP_000121.2:p.Asp1143Tyr