Canonical Allele Identifier: CA1519937710

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284063_186284064delinsAG , CM000666.2:g.186284063_186284064delinsAG	GRCh38
NC_000004.11:g.187205217_187205218delinsAG , CM000666.1:g.187205217_187205218delinsAG	GRCh37
NC_000004.10:g.187442211_187442212delinsAG	NCBI36
NG_008051.1:g.23100_23101delinsAG , LRG_583:g.23100_23101delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-29_1136-28delinsAG MANE Select	ENSP00000384957.2:n.1136-29_1136-28delins...
ENST00000264692.8:c.974-29_974-28delinsAG	ENSP00000264692.5:n.974-29_974-28delinsAG...
ENST00000403665.6:c.1136-29_1136-28delinsAG	ENSP00000384957.2:n.1136-29_1136-28delins...
NM_000128.3:c.1136-29_1136-28delinsAG , LRG_583t1:c.1136-29_1136-28delinsAG	NP_000119.1:n.1136-29_1136-28delinsAG
XM_005262821.2:c.1139-29_1139-28delinsAG	XP_005262878.1:n.1139-29_1139-28delinsAG
XM_005262822.2:c.1139-29_1139-28delinsAG	XP_005262879.1:n.1139-29_1139-28delinsAG
XM_005262823.2:c.869-29_869-28delinsAG	XP_005262880.1:n.869-29_869-28delinsAG
XM_005262824.1:c.1139-29_1139-28delinsAG	XP_005262881.1:n.1139-29_1139-28delinsAG
XM_006714137.1:c.1091-29_1091-28delinsAG	XP_006714200.1:n.1091-29_1091-28delinsAG
XR_938706.1:n.1544-29_1544-28delinsAG
XR_938707.1:n.1544-29_1544-28delinsAG
XM_005262821.4:c.1139-29_1139-28delinsAG	XP_005262878.1:n.1139-29_1139-28delinsAG
XM_005262822.4:c.1139-29_1139-28delinsAG	XP_005262879.1:n.1139-29_1139-28delinsAG
XM_005262823.4:c.869-29_869-28delinsAG	XP_005262880.1:n.869-29_869-28delinsAG
XM_006714137.3:c.1091-29_1091-28delinsAG	XP_006714200.1:n.1091-29_1091-28delinsAG
XM_017007884.2:c.*2079_*2080delinsAG	XP_016863373.1:n.*2079_*2080delinsAG
XM_017007885.2:c.*4-29_*4-28delinsAG	XP_016863374.1:n.*4-29_*4-28delinsAG
XR_001741172.2:n.1610-29_1610-28delinsAG
NM_000128.4:c.1136-29_1136-28delinsAG MANE Select	NP_000119.1:n.1136-29_1136-28delinsAG