Canonical Allele Identifier: CA1519938417

Gene: F11

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285497A= , CM000666.2:g.186285497A=	GRCh38
NC_000004.11:g.187206651A= , CM000666.1:g.187206651A=	GRCh37
NC_000004.10:g.187443645A=	NCBI36
NG_008051.1:g.24534A= , LRG_583:g.24534A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1305-141A= MANE Select	ENSP00000384957.2:n.1305-141A=
ENST00000264692.8:c.1143-141A=	ENSP00000264692.5:n.1143-141A=
ENST00000403665.6:c.1305-141A=	ENSP00000384957.2:n.1305-141A=
NM_000128.3:c.1305-141A= , LRG_583t1:c.1305-141A=	NP_000119.1:n.1305-141A=
XM_005262821.2:c.1308-141A=	XP_005262878.1:n.1308-141A=
XM_005262822.2:c.1308-141A=	XP_005262879.1:n.1308-141A=
XM_005262823.2:c.1038-141A=	XP_005262880.1:n.1038-141A=
XM_005262824.1:c.1308-141A=	XP_005262881.1:n.1308-141A=
XM_006714137.1:c.1260-141A=	XP_006714200.1:n.1260-141A=
XR_938706.1:n.1713-141A=
XR_938707.1:n.1713-141A=
XM_005262821.4:c.1308-141A=	XP_005262878.1:n.1308-141A=
XM_005262822.4:c.1308-141A=	XP_005262879.1:n.1308-141A=
XM_005262823.4:c.1038-141A=	XP_005262880.1:n.1038-141A=
XM_006714137.3:c.1260-141A=	XP_006714200.1:n.1260-141A=
XR_001741172.2:n.1779-141A=
NM_000128.4:c.1305-141A= MANE Select	NP_000119.1:n.1305-141A=