Canonical Allele Identifier: CA1519937682

Gene: F11

Linked Data

• dbSNP Id: rs1740983356
• gnomAD v4: 4-186284010-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284016_186284018del , CM000666.2:g.186284016_186284018del	GRCh38
NC_000004.11:g.187205170_187205172del , CM000666.1:g.187205170_187205172del	GRCh37
NC_000004.10:g.187442164_187442166del	NCBI36
NG_008051.1:g.23053_23055del , LRG_583:g.23053_23055del

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1136-76_1136-74del MANE Select	ENSP00000384957.2:n.1136-76_1136-74del
ENST00000264692.8:c.974-76_974-74del	ENSP00000264692.5:n.974-76_974-74del
ENST00000403665.6:c.1136-76_1136-74del	ENSP00000384957.2:n.1136-76_1136-74del
NM_000128.3:c.1136-76_1136-74del , LRG_583t1:c.1136-76_1136-74del	NP_000119.1:n.1136-76_1136-74del
XM_005262821.2:c.1139-76_1139-74del	XP_005262878.1:n.1139-76_1139-74del
XM_005262822.2:c.1139-76_1139-74del	XP_005262879.1:n.1139-76_1139-74del
XM_005262823.2:c.869-76_869-74del	XP_005262880.1:n.869-76_869-74del
XM_005262824.1:c.1139-76_1139-74del	XP_005262881.1:n.1139-76_1139-74del
XM_006714137.1:c.1091-76_1091-74del	XP_006714200.1:n.1091-76_1091-74del
XR_938706.1:n.1544-76_1544-74del
XR_938707.1:n.1544-76_1544-74del
XM_005262821.4:c.1139-76_1139-74del	XP_005262878.1:n.1139-76_1139-74del
XM_005262822.4:c.1139-76_1139-74del	XP_005262879.1:n.1139-76_1139-74del
XM_005262823.4:c.869-76_869-74del	XP_005262880.1:n.869-76_869-74del
XM_006714137.3:c.1091-76_1091-74del	XP_006714200.1:n.1091-76_1091-74del
XM_017007884.2:c.*2032_*2034del	XP_016863373.1:n.*2032_*2034del
XM_017007885.2:c.*4-76_*4-74del	XP_016863374.1:n.*4-76_*4-74del
XR_001741172.2:n.1610-76_1610-74del
NM_000128.4:c.1136-76_1136-74del MANE Select	NP_000119.1:n.1136-76_1136-74del