Canonical Allele Identifier: CA2649036202
Gene: F5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552851_169552852insTGACTTTTATCAGTGATGCAGGAGAC , CM000663.2:g.169552851_169552852insTGACTTTTATCAGTGATGCAGGAGAC GRCh38
NC_000001.10:g.169522089_169522090insTGACTTTTATCAGTGATGCAGGAGAC , CM000663.1:g.169522089_169522090insTGACTTTTATCAGTGATGCAGGAGAC GRCh37
NC_000001.9:g.167788713_167788714insTGACTTTTATCAGTGATGCAGGAGAC NCBI36
NG_011806.1:g.38680_38681insGTCTCCTGCATCACTGATAAAAGTCA , LRG_553:g.38680_38681insGTCTCCTGCATCACTGATAAAAGTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA MANE Select ENSP00000356771.3:n.1119-118_1119-117insGTCTCCTGCATCACTGATAAA...
ENST00000367796.3:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA ENSP00000356770.3:n.1119-118_1119-117insGTCTCCTGCATCACTGATAAA...
ENST00000367797.7:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA ENSP00000356771.3:n.1119-118_1119-117insGTCTCCTGCATCACTGATAAA...
NM_000130.4:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA , LRG_553t1:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA NP_000121.2:n.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA
XM_017000660.2:c.708-118_708-117insGTCTCCTGCATCACTGATAAAAGTCA XP_016856149.1:n.708-118_708-117insGTCTCCTGCATCACTGATAAAAGTCA...
NM_000130.5:c.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA MANE Select NP_000121.2:n.1119-118_1119-117insGTCTCCTGCATCACTGATAAAAGTCA