Canonical Allele Identifier: CA1519937666

Gene: F11

Linked Data

• dbSNP Id: rs1740981195

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283980_186283981insA , CM000666.2:g.186283980_186283981insA	GRCh38
NC_000004.11:g.187205134_187205135insA , CM000666.1:g.187205134_187205135insA	GRCh37
NC_000004.10:g.187442128_187442129insA	NCBI36
NG_008051.1:g.23017_23018insA , LRG_583:g.23017_23018insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-112_1136-111insA MANE Select	ENSP00000384957.2:n.1136-112_1136-111insA
ENST00000264692.8:c.974-112_974-111insA	ENSP00000264692.5:n.974-112_974-111insA
ENST00000403665.6:c.1136-112_1136-111insA	ENSP00000384957.2:n.1136-112_1136-111insA
NM_000128.3:c.1136-112_1136-111insA , LRG_583t1:c.1136-112_1136-111insA	NP_000119.1:n.1136-112_1136-111insA
XM_005262821.2:c.1139-112_1139-111insA	XP_005262878.1:n.1139-112_1139-111insA
XM_005262822.2:c.1139-112_1139-111insA	XP_005262879.1:n.1139-112_1139-111insA
XM_005262823.2:c.869-112_869-111insA	XP_005262880.1:n.869-112_869-111insA
XM_005262824.1:c.1139-112_1139-111insA	XP_005262881.1:n.1139-112_1139-111insA
XM_006714137.1:c.1091-112_1091-111insA	XP_006714200.1:n.1091-112_1091-111insA
XR_938706.1:n.1544-112_1544-111insA
XR_938707.1:n.1544-112_1544-111insA
XM_005262821.4:c.1139-112_1139-111insA	XP_005262878.1:n.1139-112_1139-111insA
XM_005262822.4:c.1139-112_1139-111insA	XP_005262879.1:n.1139-112_1139-111insA
XM_005262823.4:c.869-112_869-111insA	XP_005262880.1:n.869-112_869-111insA
XM_006714137.3:c.1091-112_1091-111insA	XP_006714200.1:n.1091-112_1091-111insA
XM_017007884.2:c.*1996_*1997insA	XP_016863373.1:n.*1996_*1997insA
XM_017007885.2:c.*4-112_*4-111insA	XP_016863374.1:n.*4-112_*4-111insA
XR_001741172.2:n.1610-112_1610-111insA
NM_000128.4:c.1136-112_1136-111insA MANE Select	NP_000119.1:n.1136-112_1136-111insA