Canonical Allele Identifier: CA2571826845
Gene: F5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169530617_169530618insAAGTCAAGACTCCTTTATCTGACATTCTGCAA , CM000663.2:g.169530617_169530618insAAGTCAAGACTCCTTTATCTGACATTCTGCAA GRCh38
NC_000001.10:g.169499855_169499856insAAGTCAAGACTCCTTTATCTGACATTCTGCAA , CM000663.1:g.169499855_169499856insAAGTCAAGACTCCTTTATCTGACATTCTGCAA GRCh37
NC_000001.9:g.167766479_167766480insAAGTCAAGACTCCTTTATCTGACATTCTGCAA NCBI36
NG_011806.1:g.60915_60916insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT , LRG_553:g.60915_60916insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5208+169_5208+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT MANE Select ENSP00000356771.3:n.5208+169_5208+170insT...
ENST00000367796.3:c.5223+169_5223+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT ENSP00000356770.3:n.5223+169_5223+170insT...
ENST00000367797.7:c.5208+169_5208+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT ENSP00000356771.3:n.5208+169_5208+170insT...
NM_000130.4:c.5208+169_5208+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT , LRG_553t1:c.5208+169_5208+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT NP_000121.2:n.5208+169_5208+170insTGCAGAA...
XM_017000660.2:c.4797+169_4797+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT XP_016856149.1:n.4797+169_4797+170insTGCA...
NM_000130.5:c.5208+169_5208+170insTGCAGAATGTCAGATAAAGGAGTCTTGACTTT MANE Select NP_000121.2:n.5208+169_5208+170insTGCAGAA...