Canonical Allele Identifier: CA112153126

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276603_186276604del , CM000666.2:g.186276603_186276604del	GRCh38
NC_000004.11:g.187197757_187197758del , CM000666.1:g.187197757_187197758del	GRCh37
NC_000004.10:g.187434751_187434752del	NCBI36
NG_008051.1:g.15640_15641del , LRG_583:g.15640_15641del

Transcript Alleles

HGVS	Amino-acid Change
NM_000128.4:c.755+213_755+214del MANE Select	NP_000119.1:n.755+213_755+214del
ENST00000403665.7:c.755+213_755+214del MANE Select	ENSP00000384957.2:n.755+213_755+214del
NM_000128.3:c.755+213_755+214del , LRG_583t1:c.755+213_755+214del	NP_000119.1:n.755+213_755+214del
ENST00000264692.8:c.593+213_593+214del	ENSP00000264692.5:n.593+213_593+214del
ENST00000403665.6:c.755+213_755+214del	ENSP00000384957.2:n.755+213_755+214del
ENST00000452239.1:c.202+213_202+214del
XM_005262821.2:c.755+213_755+214del	XP_005262878.1:n.755+213_755+214del
XM_005262821.4:c.755+213_755+214del	XP_005262878.1:n.755+213_755+214del
XM_005262822.2:c.755+213_755+214del	XP_005262879.1:n.755+213_755+214del
XM_005262822.4:c.755+213_755+214del	XP_005262879.1:n.755+213_755+214del
XM_005262823.2:c.485+2328_485+2329del	XP_005262880.1:n.485+2328_485+2329del
XM_005262823.4:c.485+2328_485+2329del	XP_005262880.1:n.485+2328_485+2329del
XM_005262824.1:c.755+213_755+214del	XP_005262881.1:n.755+213_755+214del
XM_006714137.1:c.755+213_755+214del	XP_006714200.1:n.755+213_755+214del
XM_006714137.3:c.755+213_755+214del	XP_006714200.1:n.755+213_755+214del
XM_017007884.2:c.755+213_755+214del	XP_016863373.1:n.755+213_755+214del
XM_017007885.2:c.755+213_755+214del	XP_016863374.1:n.755+213_755+214del
XM_017007886.2:c.755+213_755+214del	XP_016863375.1:n.755+213_755+214del
XR_001741172.2:n.1088+213_1088+214del
XR_938706.1:n.1107+213_1107+214del
XR_938707.1:n.1107+213_1107+214del