Canonical Allele Identifier: CA343130975
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555207G>C , CM000663.2:g.169555207G>C GRCh38
NC_000001.10:g.169524445G>C , CM000663.1:g.169524445G>C GRCh37
NC_000001.9:g.167791069G>C NCBI36
NG_011806.1:g.36325C>G , LRG_553:g.36325C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.1093C>G MANE Select ENSP00000356771.3:p.Pro365Ala
ENST00000367796.3:c.1093C>G ENSP00000356770.3:p.Pro365Ala
ENST00000367797.7:c.1093C>G ENSP00000356771.3:p.Pro365Ala
NM_000130.4:c.1093C>G , LRG_553t1:c.1093C>G NP_000121.2:p.Pro365Ala
XM_017000660.2:c.682C>G XP_016856149.1:p.Pro228Ala
NM_000130.5:c.1093C>G MANE Select NP_000121.2:p.Pro365Ala