Canonical Allele Identifier: CA1206149453
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555375_169555380delinsTAACTC , CM000663.2:g.169555375_169555380delinsTAACTC GRCh38
NC_000001.10:g.169524613_169524618delinsTAACTC , CM000663.1:g.169524613_169524618delinsTAACTC GRCh37
NC_000001.9:g.167791237_167791242delinsTAACTC NCBI36
NG_011806.1:g.36152_36157delinsGAGTTA , LRG_553:g.36152_36157delinsGAGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.953-33_953-28delinsGAGTTA MANE Select ENSP00000356771.3:n.953-33_953-28delinsGAGTTA
ENST00000367796.3:c.953-33_953-28delinsGAGTTA ENSP00000356770.3:n.953-33_953-28delinsGAGTTA
ENST00000367797.7:c.953-33_953-28delinsGAGTTA ENSP00000356771.3:n.953-33_953-28delinsGAGTTA
NM_000130.4:c.953-33_953-28delinsGAGTTA , LRG_553t1:c.953-33_953-28delinsGAGTTA NP_000121.2:n.953-33_953-28delinsGAGTTA
XM_017000660.2:c.542-33_542-28delinsGAGTTA XP_016856149.1:n.542-33_542-28delinsGAGTTA
NM_000130.5:c.953-33_953-28delinsGAGTTA MANE Select NP_000121.2:n.953-33_953-28delinsGAGTTA