Canonical Allele Identifier: CA1519935846

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186279972_186279977delinsTTGATA , CM000666.2:g.186279972_186279977delinsTTGATA	GRCh38
NC_000004.11:g.187201126_187201131delinsTTGATA , CM000666.1:g.187201126_187201131delinsTTGATA	GRCh37
NC_000004.10:g.187438120_187438125delinsTTGATA	NCBI36
NG_008051.1:g.19009_19014delinsTTGATA , LRG_583:g.19009_19014delinsTTGATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.756-40_756-35delinsTTGATA MANE Select	ENSP00000384957.2:n.756-40_756-35delinsTT...
ENST00000264692.8:c.594-40_594-35delinsTTGATA	ENSP00000264692.5:n.594-40_594-35delinsTT...
ENST00000403665.6:c.756-40_756-35delinsTTGATA	ENSP00000384957.2:n.756-40_756-35delinsTT...
ENST00000452239.1:c.203-40_203-35delinsTTGATA
NM_000128.3:c.756-40_756-35delinsTTGATA , LRG_583t1:c.756-40_756-35delinsTTGATA	NP_000119.1:n.756-40_756-35delinsTTGATA
XM_005262821.2:c.756-40_756-35delinsTTGATA	XP_005262878.1:n.756-40_756-35delinsTTGAT...
XM_005262822.2:c.756-40_756-35delinsTTGATA	XP_005262879.1:n.756-40_756-35delinsTTGAT...
XM_005262823.2:c.486-40_486-35delinsTTGATA	XP_005262880.1:n.486-40_486-35delinsTTGAT...
XM_005262824.1:c.756-40_756-35delinsTTGATA	XP_005262881.1:n.756-40_756-35delinsTTGAT...
XM_006714137.1:c.756-40_756-35delinsTTGATA	XP_006714200.1:n.756-40_756-35delinsTTGAT...
XR_938706.1:n.1108-40_1108-35delinsTTGATA
XR_938707.1:n.1108-40_1108-35delinsTTGATA
XM_005262821.4:c.756-40_756-35delinsTTGATA	XP_005262878.1:n.756-40_756-35delinsTTGAT...
XM_005262822.4:c.756-40_756-35delinsTTGATA	XP_005262879.1:n.756-40_756-35delinsTTGAT...
XM_005262823.4:c.486-40_486-35delinsTTGATA	XP_005262880.1:n.486-40_486-35delinsTTGAT...
XM_006714137.3:c.756-40_756-35delinsTTGATA	XP_006714200.1:n.756-40_756-35delinsTTGAT...
XM_017007884.2:c.756-40_756-35delinsTTGATA	XP_016863373.1:n.756-40_756-35delinsTTGAT...
XM_017007885.2:c.756-40_756-35delinsTTGATA	XP_016863374.1:n.756-40_756-35delinsTTGAT...
XM_017007886.2:c.756-40_756-35delinsTTGATA	XP_016863375.1:n.756-40_756-35delinsTTGAT...
XR_001741172.2:n.1089-40_1089-35delinsTTGATA
NM_000128.4:c.756-40_756-35delinsTTGATA MANE Select	NP_000119.1:n.756-40_756-35delinsTTGATA