Canonical Allele Identifier: CA1519937681

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284010_186284013delinsTTTC , CM000666.2:g.186284010_186284013delinsTTTC	GRCh38
NC_000004.11:g.187205164_187205167delinsTTTC , CM000666.1:g.187205164_187205167delinsTTTC	GRCh37
NC_000004.10:g.187442158_187442161delinsTTTC	NCBI36
NG_008051.1:g.23047_23050delinsTTTC , LRG_583:g.23047_23050delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-82_1136-79delinsTTTC MANE Select	ENSP00000384957.2:n.1136-82_1136-79delinsTTTC
ENST00000264692.8:c.974-82_974-79delinsTTTC	ENSP00000264692.5:n.974-82_974-79delinsTTTC
ENST00000403665.6:c.1136-82_1136-79delinsTTTC	ENSP00000384957.2:n.1136-82_1136-79delinsTTTC
NM_000128.3:c.1136-82_1136-79delinsTTTC , LRG_583t1:c.1136-82_1136-79delinsTTTC	NP_000119.1:n.1136-82_1136-79delinsTTTC
XM_005262821.2:c.1139-82_1139-79delinsTTTC	XP_005262878.1:n.1139-82_1139-79delinsTTTC
XM_005262822.2:c.1139-82_1139-79delinsTTTC	XP_005262879.1:n.1139-82_1139-79delinsTTTC
XM_005262823.2:c.869-82_869-79delinsTTTC	XP_005262880.1:n.869-82_869-79delinsTTTC
XM_005262824.1:c.1139-82_1139-79delinsTTTC	XP_005262881.1:n.1139-82_1139-79delinsTTTC
XM_006714137.1:c.1091-82_1091-79delinsTTTC	XP_006714200.1:n.1091-82_1091-79delinsTTTC
XR_938706.1:n.1544-82_1544-79delinsTTTC
XR_938707.1:n.1544-82_1544-79delinsTTTC
XM_005262821.4:c.1139-82_1139-79delinsTTTC	XP_005262878.1:n.1139-82_1139-79delinsTTTC
XM_005262822.4:c.1139-82_1139-79delinsTTTC	XP_005262879.1:n.1139-82_1139-79delinsTTTC
XM_005262823.4:c.869-82_869-79delinsTTTC	XP_005262880.1:n.869-82_869-79delinsTTTC
XM_006714137.3:c.1091-82_1091-79delinsTTTC	XP_006714200.1:n.1091-82_1091-79delinsTTTC
XM_017007884.2:c.*2026_*2029delinsTTTC	XP_016863373.1:n.*2026_*2029delinsTTTC
XM_017007885.2:c.*4-82_*4-79delinsTTTC	XP_016863374.1:n.*4-82_*4-79delinsTTTC
XR_001741172.2:n.1610-82_1610-79delinsTTTC
NM_000128.4:c.1136-82_1136-79delinsTTTC MANE Select	NP_000119.1:n.1136-82_1136-79delinsTTTC