Canonical Allele Identifier: CA792306570

Gene: F11

Linked Data

• dbSNP Id: rs1310213450
• MyVariant Identifiers: chr4:g.187195709_187195714del (hg19) ; chr4:g.186274555_186274560del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186274557_186274562del , CM000666.2:g.186274557_186274562del	GRCh38
NC_000004.11:g.187195711_187195716del , CM000666.1:g.187195711_187195716del	GRCh37
NC_000004.10:g.187432705_187432710del	NCBI36
NG_008051.1:g.13594_13599del , LRG_583:g.13594_13599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.485+282_485+287del MANE Select	ENSP00000384957.2:n.485+282_485+287del
ENST00000264692.8:c.324-1230_324-1225del	ENSP00000264692.5:n.324-1230_324-1225del
ENST00000403665.6:c.485+282_485+287del	ENSP00000384957.2:n.485+282_485+287del
ENST00000492972.6:c.*278_*283del	ENSP00000424479.1:n.*278_*283del
ENST00000514715.1:n.639_644del
NM_000128.3:c.485+282_485+287del , LRG_583t1:c.485+282_485+287del	NP_000119.1:n.485+282_485+287del
XM_005262821.2:c.485+282_485+287del	XP_005262878.1:n.485+282_485+287del
XM_005262822.2:c.485+282_485+287del	XP_005262879.1:n.485+282_485+287del
XM_005262823.2:c.485+282_485+287del	XP_005262880.1:n.485+282_485+287del
XM_005262824.1:c.485+282_485+287del	XP_005262881.1:n.485+282_485+287del
XM_006714137.1:c.485+282_485+287del	XP_006714200.1:n.485+282_485+287del
XR_938706.1:n.837+282_837+287del
XR_938707.1:n.837+282_837+287del
NM_001354804.1:c.*278_*283del	NP_001341733.1:n.*278_*283del
XM_005262821.4:c.485+282_485+287del	XP_005262878.1:n.485+282_485+287del
XM_005262822.4:c.485+282_485+287del	XP_005262879.1:n.485+282_485+287del
XM_005262823.4:c.485+282_485+287del	XP_005262880.1:n.485+282_485+287del
XM_006714137.3:c.485+282_485+287del	XP_006714200.1:n.485+282_485+287del
XM_017007884.2:c.485+282_485+287del	XP_016863373.1:n.485+282_485+287del
XM_017007885.2:c.485+282_485+287del	XP_016863374.1:n.485+282_485+287del
XM_017007886.2:c.485+282_485+287del	XP_016863375.1:n.485+282_485+287del
XR_001741172.2:n.818+282_818+287del
NM_000128.4:c.485+282_485+287del MANE Select	NP_000119.1:n.485+282_485+287del
NM_001354804.2:c.*278_*283del	NP_001341733.1:n.*278_*283del