Canonical Allele Identifier: CA1519937985

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284623_186284627delinsATGTG , CM000666.2:g.186284623_186284627delinsATGTG	GRCh38
NC_000004.11:g.187205777_187205781delinsATGTG , CM000666.1:g.187205777_187205781delinsATGTG	GRCh37
NC_000004.10:g.187442771_187442775delinsATGTG	NCBI36
NG_008051.1:g.23660_23664delinsATGTG , LRG_583:g.23660_23664delinsATGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1304+363_1304+367delinsATGTG MANE Select	ENSP00000384957.2:n.1304+363_1304+367delinsATGTG
ENST00000264692.8:c.1142+363_1142+367delinsATGTG	ENSP00000264692.5:n.1142+363_1142+367delinsATGTG
ENST00000403665.6:c.1304+363_1304+367delinsATGTG	ENSP00000384957.2:n.1304+363_1304+367delinsATGTG
NM_000128.3:c.1304+363_1304+367delinsATGTG , LRG_583t1:c.1304+363_1304+367delinsATGTG	NP_000119.1:n.1304+363_1304+367delinsATGTG
XM_005262821.2:c.1307+363_1307+367delinsATGTG	XP_005262878.1:n.1307+363_1307+367delinsATGTG
XM_005262822.2:c.1307+363_1307+367delinsATGTG	XP_005262879.1:n.1307+363_1307+367delinsATGTG
XM_005262823.2:c.1037+363_1037+367delinsATGTG	XP_005262880.1:n.1037+363_1037+367delinsATGTG
XM_005262824.1:c.1307+363_1307+367delinsATGTG	XP_005262881.1:n.1307+363_1307+367delinsATGTG
XM_006714137.1:c.1259+363_1259+367delinsATGTG	XP_006714200.1:n.1259+363_1259+367delinsATGTG
XR_938706.1:n.1712+363_1712+367delinsATGTG
XR_938707.1:n.1712+363_1712+367delinsATGTG
XM_005262821.4:c.1307+363_1307+367delinsATGTG	XP_005262878.1:n.1307+363_1307+367delinsATGTG
XM_005262822.4:c.1307+363_1307+367delinsATGTG	XP_005262879.1:n.1307+363_1307+367delinsATGTG
XM_005262823.4:c.1037+363_1037+367delinsATGTG	XP_005262880.1:n.1037+363_1037+367delinsATGTG
XM_006714137.3:c.1259+363_1259+367delinsATGTG	XP_006714200.1:n.1259+363_1259+367delinsATGTG
XR_001741172.2:n.1778+363_1778+367delinsATGTG
NM_000128.4:c.1304+363_1304+367delinsATGTG MANE Select	NP_000119.1:n.1304+363_1304+367delinsATGTG