Canonical Allele Identifier: CA1519934299

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276542T= , CM000666.2:g.186276542T=	GRCh38
NC_000004.11:g.187197696T= , CM000666.1:g.187197696T=	GRCh37
NC_000004.10:g.187434690T=	NCBI36
NG_008051.1:g.15579T= , LRG_583:g.15579T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.755+152T= MANE Select	ENSP00000384957.2:n.755+152T=
ENST00000264692.8:c.593+152T=	ENSP00000264692.5:n.593+152T=
ENST00000403665.6:c.755+152T=	ENSP00000384957.2:n.755+152T=
ENST00000452239.1:c.202+152T=
NM_000128.3:c.755+152T= , LRG_583t1:c.755+152T=	NP_000119.1:n.755+152T=
XM_005262821.2:c.755+152T=	XP_005262878.1:n.755+152T=
XM_005262822.2:c.755+152T=	XP_005262879.1:n.755+152T=
XM_005262823.2:c.485+2267T=	XP_005262880.1:n.485+2267T=
XM_005262824.1:c.755+152T=	XP_005262881.1:n.755+152T=
XM_006714137.1:c.755+152T=	XP_006714200.1:n.755+152T=
XR_938706.1:n.1107+152T=
XR_938707.1:n.1107+152T=
XM_005262821.4:c.755+152T=	XP_005262878.1:n.755+152T=
XM_005262822.4:c.755+152T=	XP_005262879.1:n.755+152T=
XM_005262823.4:c.485+2267T=	XP_005262880.1:n.485+2267T=
XM_006714137.3:c.755+152T=	XP_006714200.1:n.755+152T=
XM_017007884.2:c.755+152T=	XP_016863373.1:n.755+152T=
XM_017007885.2:c.755+152T=	XP_016863374.1:n.755+152T=
XM_017007886.2:c.755+152T=	XP_016863375.1:n.755+152T=
XR_001741172.2:n.1088+152T=
NM_000128.4:c.755+152T= MANE Select	NP_000119.1:n.755+152T=