Canonical Allele Identifier: CA1519937684

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284018_186284019delinsTG , CM000666.2:g.186284018_186284019delinsTG	GRCh38
NC_000004.11:g.187205172_187205173delinsTG , CM000666.1:g.187205172_187205173delinsTG	GRCh37
NC_000004.10:g.187442166_187442167delinsTG	NCBI36
NG_008051.1:g.23055_23056delinsTG , LRG_583:g.23055_23056delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1136-74_1136-73delinsTG MANE Select	ENSP00000384957.2:n.1136-74_1136-73delinsTG
ENST00000264692.8:c.974-74_974-73delinsTG	ENSP00000264692.5:n.974-74_974-73delinsTG
ENST00000403665.6:c.1136-74_1136-73delinsTG	ENSP00000384957.2:n.1136-74_1136-73delinsTG
NM_000128.3:c.1136-74_1136-73delinsTG , LRG_583t1:c.1136-74_1136-73delinsTG	NP_000119.1:n.1136-74_1136-73delinsTG
XM_005262821.2:c.1139-74_1139-73delinsTG	XP_005262878.1:n.1139-74_1139-73delinsTG
XM_005262822.2:c.1139-74_1139-73delinsTG	XP_005262879.1:n.1139-74_1139-73delinsTG
XM_005262823.2:c.869-74_869-73delinsTG	XP_005262880.1:n.869-74_869-73delinsTG
XM_005262824.1:c.1139-74_1139-73delinsTG	XP_005262881.1:n.1139-74_1139-73delinsTG
XM_006714137.1:c.1091-74_1091-73delinsTG	XP_006714200.1:n.1091-74_1091-73delinsTG
XR_938706.1:n.1544-74_1544-73delinsTG
XR_938707.1:n.1544-74_1544-73delinsTG
XM_005262821.4:c.1139-74_1139-73delinsTG	XP_005262878.1:n.1139-74_1139-73delinsTG
XM_005262822.4:c.1139-74_1139-73delinsTG	XP_005262879.1:n.1139-74_1139-73delinsTG
XM_005262823.4:c.869-74_869-73delinsTG	XP_005262880.1:n.869-74_869-73delinsTG
XM_006714137.3:c.1091-74_1091-73delinsTG	XP_006714200.1:n.1091-74_1091-73delinsTG
XM_017007884.2:c.*2034_*2035delinsTG	XP_016863373.1:n.*2034_*2035delinsTG
XM_017007885.2:c.*4-74_*4-73delinsTG	XP_016863374.1:n.*4-74_*4-73delinsTG
XR_001741172.2:n.1610-74_1610-73delinsTG
NM_000128.4:c.1136-74_1136-73delinsTG MANE Select	NP_000119.1:n.1136-74_1136-73delinsTG