Canonical Allele Identifier: CA2740197713
Gene: F5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169549626dup , CM000663.2:g.169549626dup GRCh38
NC_000001.10:g.169518864dup , CM000663.1:g.169518864dup GRCh37
NC_000001.9:g.167785488dup NCBI36
NG_011806.1:g.41906dup , LRG_553:g.41906dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1611+175dup MANE Select ENSP00000356771.3:n.1611+175dup
ENST00000367796.3:c.1611+175dup ENSP00000356770.3:n.1611+175dup
ENST00000367797.7:c.1611+175dup ENSP00000356771.3:n.1611+175dup
NM_000130.4:c.1611+175dup , LRG_553t1:c.1611+175dup NP_000121.2:n.1611+175dup
XM_017000660.2:c.1200+175dup XP_016856149.1:n.1200+175dup
NM_000130.5:c.1611+175dup MANE Select NP_000121.2:n.1611+175dup
Search 100 bp 5'
Search 100 bp 3'