Canonical Allele Identifier: CA2649036468
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555306dup , CM000663.2:g.169555306dup GRCh38
NC_000001.10:g.169524544dup , CM000663.1:g.169524544dup GRCh37
NC_000001.9:g.167791168dup NCBI36
NG_011806.1:g.36229dup , LRG_553:g.36229dup

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.997dup MANE Select ENSP00000356771.3:p.Thr333AsnfsTer5
ENST00000367796.3:c.997dup ENSP00000356770.3:p.Thr333AsnfsTer5
ENST00000367797.7:c.997dup ENSP00000356771.3:p.Thr333AsnfsTer5
NM_000130.4:c.997dup , LRG_553t1:c.997dup NP_000121.2:p.Thr333AsnfsTer5
XM_017000660.2:c.586dup XP_016856149.1:p.Thr196AsnfsTer5
NM_000130.5:c.997dup MANE Select NP_000121.2:p.Thr333AsnfsTer5