Canonical Allele Identifier: CA1519938557

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285816_186285830delinsACGGAGAATTTTATC , CM000666.2:g.186285816_186285830delinsACGGAGAATTTTATC	GRCh38
NC_000004.11:g.187206970_187206984delinsACGGAGAATTTTATC , CM000666.1:g.187206970_187206984delinsACGGAGAATTTTATC	GRCh37
NC_000004.10:g.187443964_187443978delinsACGGAGAATTTTATC	NCBI36
NG_008051.1:g.24853_24867delinsACGGAGAATTTTATC , LRG_583:g.24853_24867delinsACGGAGAATTTTATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1480+3_1480+17delinsACGGAGAATTTTATC MANE Select	ENSP00000384957.2:n.1480+3_1480+17delinsACGGAGAATTTTATC
ENST00000264691.4:c.176+3_176+17delinsACGGAGAATTTTATC
ENST00000264692.8:c.1318+3_1318+17delinsACGGAGAATTTTATC	ENSP00000264692.5:n.1318+3_1318+17delinsACGGAGAATTTTATC
ENST00000403665.6:c.1480+3_1480+17delinsACGGAGAATTTTATC	ENSP00000384957.2:n.1480+3_1480+17delinsACGGAGAATTTTATC
NM_000128.3:c.1480+3_1480+17delinsACGGAGAATTTTATC , LRG_583t1:c.1480+3_1480+17delinsACGGAGAATTTTATC	NP_000119.1:n.1480+3_1480+17delinsACGGAGAATTTTATC
XM_005262821.2:c.1483+3_1483+17delinsACGGAGAATTTTATC	XP_005262878.1:n.1483+3_1483+17delinsACGGAGAATTTTATC
XM_005262822.2:c.1483+3_1483+17delinsACGGAGAATTTTATC	XP_005262879.1:n.1483+3_1483+17delinsACGGAGAATTTTATC
XM_005262823.2:c.1213+3_1213+17delinsACGGAGAATTTTATC	XP_005262880.1:n.1213+3_1213+17delinsACGGAGAATTTTATC
XM_005262824.1:c.1483+3_1483+17delinsACGGAGAATTTTATC	XP_005262881.1:n.1483+3_1483+17delinsACGGAGAATTTTATC
XM_006714137.1:c.1435+3_1435+17delinsACGGAGAATTTTATC	XP_006714200.1:n.1435+3_1435+17delinsACGGAGAATTTTATC
XR_938706.1:n.1888+3_1888+17delinsACGGAGAATTTTATC
XR_938707.1:n.1888+3_1888+17delinsACGGAGAATTTTATC
XM_005262821.4:c.1483+3_1483+17delinsACGGAGAATTTTATC	XP_005262878.1:n.1483+3_1483+17delinsACGGAGAATTTTATC
XM_005262822.4:c.1483+3_1483+17delinsACGGAGAATTTTATC	XP_005262879.1:n.1483+3_1483+17delinsACGGAGAATTTTATC
XM_005262823.4:c.1213+3_1213+17delinsACGGAGAATTTTATC	XP_005262880.1:n.1213+3_1213+17delinsACGGAGAATTTTATC
XM_006714137.3:c.1435+3_1435+17delinsACGGAGAATTTTATC	XP_006714200.1:n.1435+3_1435+17delinsACGGAGAATTTTATC
XR_001741172.2:n.1954+3_1954+17delinsACGGAGAATTTTATC
NM_000128.4:c.1480+3_1480+17delinsACGGAGAATTTTATC MANE Select	NP_000119.1:n.1480+3_1480+17delinsACGGAGAATTTTATC