Canonical Allele Identifier: CA1519937667

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186283982_186283983delinsAT , CM000666.2:g.186283982_186283983delinsAT	GRCh38
NC_000004.11:g.187205136_187205137delinsAT , CM000666.1:g.187205136_187205137delinsAT	GRCh37
NC_000004.10:g.187442130_187442131delinsAT	NCBI36
NG_008051.1:g.23019_23020delinsAT , LRG_583:g.23019_23020delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-110_1136-109delinsAT MANE Select	ENSP00000384957.2:n.1136-110_1136-109delinsAT
ENST00000264692.8:c.974-110_974-109delinsAT	ENSP00000264692.5:n.974-110_974-109delinsAT
ENST00000403665.6:c.1136-110_1136-109delinsAT	ENSP00000384957.2:n.1136-110_1136-109delinsAT
NM_000128.3:c.1136-110_1136-109delinsAT , LRG_583t1:c.1136-110_1136-109delinsAT	NP_000119.1:n.1136-110_1136-109delinsAT
XM_005262821.2:c.1139-110_1139-109delinsAT	XP_005262878.1:n.1139-110_1139-109delinsAT
XM_005262822.2:c.1139-110_1139-109delinsAT	XP_005262879.1:n.1139-110_1139-109delinsAT
XM_005262823.2:c.869-110_869-109delinsAT	XP_005262880.1:n.869-110_869-109delinsAT
XM_005262824.1:c.1139-110_1139-109delinsAT	XP_005262881.1:n.1139-110_1139-109delinsAT
XM_006714137.1:c.1091-110_1091-109delinsAT	XP_006714200.1:n.1091-110_1091-109delinsAT
XR_938706.1:n.1544-110_1544-109delinsAT
XR_938707.1:n.1544-110_1544-109delinsAT
XM_005262821.4:c.1139-110_1139-109delinsAT	XP_005262878.1:n.1139-110_1139-109delinsAT
XM_005262822.4:c.1139-110_1139-109delinsAT	XP_005262879.1:n.1139-110_1139-109delinsAT
XM_005262823.4:c.869-110_869-109delinsAT	XP_005262880.1:n.869-110_869-109delinsAT
XM_006714137.3:c.1091-110_1091-109delinsAT	XP_006714200.1:n.1091-110_1091-109delinsAT
XM_017007884.2:c.*1998_*1999delinsAT	XP_016863373.1:n.*1998_*1999delinsAT
XM_017007885.2:c.*4-110_*4-109delinsAT	XP_016863374.1:n.*4-110_*4-109delinsAT
XR_001741172.2:n.1610-110_1610-109delinsAT
NM_000128.4:c.1136-110_1136-109delinsAT MANE Select	NP_000119.1:n.1136-110_1136-109delinsAT