Canonical Allele Identifier: CA2672902284

Gene: F11

Linked Data

• gnomAD v4: 4-186276236-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276238dup , CM000666.2:g.186276238dup	GRCh38
NC_000004.11:g.187197392dup , CM000666.1:g.187197392dup	GRCh37
NC_000004.10:g.187434386dup	NCBI36
NG_008051.1:g.15275dup , LRG_583:g.15275dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.603dup MANE Select	ENSP00000384957.2:p.Arg202Ter
ENST00000264692.8:c.441dup	ENSP00000264692.5:p.Arg148Ter
ENST00000403665.6:c.603dup	ENSP00000384957.2:p.Arg202Ter
ENST00000452239.1:c.50dup
NM_000128.3:c.603dup , LRG_583t1:c.603dup	NP_000119.1:p.Arg202Ter
XM_005262821.2:c.603dup	XP_005262878.1:p.Arg202Ter
XM_005262822.2:c.603dup	XP_005262879.1:p.Arg202Ter
XM_005262823.2:c.485+1963dup	XP_005262880.1:n.485+1963dup
XM_005262824.1:c.603dup	XP_005262881.1:p.Arg202Ter
XM_006714137.1:c.603dup	XP_006714200.1:p.Arg202Ter
XR_938706.1:n.955dup
XR_938707.1:n.955dup
XM_005262821.4:c.603dup	XP_005262878.1:p.Arg202Ter
XM_005262822.4:c.603dup	XP_005262879.1:p.Arg202Ter
XM_005262823.4:c.485+1963dup	XP_005262880.1:n.485+1963dup
XM_006714137.3:c.603dup	XP_006714200.1:p.Arg202Ter
XM_017007884.2:c.603dup	XP_016863373.1:p.Arg202Ter
XM_017007885.2:c.603dup	XP_016863374.1:p.Arg202Ter
XM_017007886.2:c.603dup	XP_016863375.1:p.Arg202Ter
XR_001741172.2:n.936dup
NM_000128.4:c.603dup MANE Select	NP_000119.1:p.Arg202Ter