Canonical Allele Identifier: CA1519935893

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280072_186280073delinsCA , CM000666.2:g.186280072_186280073delinsCA	GRCh38
NC_000004.11:g.187201226_187201227delinsCA , CM000666.1:g.187201226_187201227delinsCA	GRCh37
NC_000004.10:g.187438220_187438221delinsCA	NCBI36
NG_008051.1:g.19109_19110delinsCA , LRG_583:g.19109_19110delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.816_817delinsCA MANE Select	ENSP00000384957.2:p.Ser272=
ENST00000264692.8:c.654_655delinsCA	ENSP00000264692.5:p.Ser218=
ENST00000403665.6:c.816_817delinsCA	ENSP00000384957.2:p.Ser272=
ENST00000452239.1:c.263_264delinsCA
NM_000128.3:c.816_817delinsCA , LRG_583t1:c.816_817delinsCA	NP_000119.1:p.Ser272=
XM_005262821.2:c.816_817delinsCA	XP_005262878.1:p.Ser272=
XM_005262822.2:c.816_817delinsCA	XP_005262879.1:p.Ser272=
XM_005262823.2:c.546_547delinsCA	XP_005262880.1:p.Ser182=
XM_005262824.1:c.816_817delinsCA	XP_005262881.1:p.Ser272=
XM_006714137.1:c.816_817delinsCA	XP_006714200.1:p.Ser272=
XR_938706.1:n.1168_1169delinsCA
XR_938707.1:n.1168_1169delinsCA
XM_005262821.4:c.816_817delinsCA	XP_005262878.1:p.Ser272=
XM_005262822.4:c.816_817delinsCA	XP_005262879.1:p.Ser272=
XM_005262823.4:c.546_547delinsCA	XP_005262880.1:p.Ser182=
XM_006714137.3:c.816_817delinsCA	XP_006714200.1:p.Ser272=
XM_017007884.2:c.816_817delinsCA	XP_016863373.1:p.Ser272=
XM_017007885.2:c.816_817delinsCA	XP_016863374.1:p.Ser272=
XM_017007886.2:c.816_817delinsCA	XP_016863375.1:p.Ser272=
XR_001741172.2:n.1149_1150delinsCA
NM_000128.4:c.816_817delinsCA MANE Select	NP_000119.1:p.Ser272=