Canonical Allele Identifier: CA2741807119

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837767_154837768insAAAGAAAAAGAAAATCAAGAGAAAGAGGAGTTGCATCACAAATATACTCACATTCC , CM000685.2:g.154837767_154837768insAAAGAAAAAGAAAATCAAGAGAAAGAGGAGTTGCATCACAAATATACTCACATTCC	GRCh38
NC_000023.10:g.154066042_154066043insAAAGAAAAAGAAAATCAAGAGAAAGAGGAGTTGCATCACAAATATACTCACATTCC , CM000685.1:g.154066042_154066043insAAAGAAAAAGAAAATCAAGAGAAAGAGGAGTTGCATCACAAATATACTCACATTCC	GRCh37
NC_000023.9:g.153719236_153719237insAAAGAAAAAGAAAATCAAGAGAAAGAGGAGTTGCATCACAAATATACTCACATTCC	NCBI36
NG_011403.1:g.189956_189957insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT
NG_033065.1:g.1895_1896insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT
NG_011403.2:g.189956_189957insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT MANE Select	ENSP00000353393.4:n.6901-16_6901-15insGGAATGTGAGTATATTTGTGATG...
ENST00000644698.1:c.634-16_634-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	ENSP00000495706.1:n.634-16_634-15insGGAATGTGAGTATATTTGTGATGCA...
ENST00000330287.10:c.496-16_496-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	ENSP00000327895.6:n.496-16_496-15insGGAATGTGAGTATATTTGTGATGCA...
ENST00000360256.8:c.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	ENSP00000353393.4:n.6901-16_6901-15insGGAATGTGAGTATATTTGTGATG...
NM_000132.3:c.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	NP_000123.1:n.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTC...
NM_019863.2:c.496-16_496-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	NP_063916.1:n.496-16_496-15insGGAATGTGAGTATATTTGTGATGCAACTCCT...
XM_011531126.1:c.6796-16_6796-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	XP_011529428.1:n.6796-16_6796-15insGGAATGTGAGTATATTTGTGATGCAA...
NM_000132.4:c.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT MANE Select	NP_000123.1:n.6901-16_6901-15insGGAATGTGAGTATATTTGTGATGCAACTC...
NM_019863.3:c.496-16_496-15insGGAATGTGAGTATATTTGTGATGCAACTCCTCTTTCTCTTGATTTTCTTTTTCTTT	NP_063916.1:n.496-16_496-15insGGAATGTGAGTATATTTGTGATGCAACTCCT...