Canonical Allele Identifier: CA1519940219

Gene: F11 F11-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186289236G= , CM000666.2:g.186289236G=	GRCh38
NC_000004.11:g.187210390G= , CM000666.1:g.187210390G=	GRCh37
NC_000004.10:g.187447384G=	NCBI36
NG_008051.1:g.28273G= , LRG_583:g.28273G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*622G= (F11) MANE Select	ENSP00000384957.2:n.*622G=
NM_000128.3:c.*622G= , LRG_583t1:c.*622G= (F11)	NP_000119.1:n.*622G=
NR_033900.1:n.492-234C= (F11-AS1)
XM_005262821.2:c.*622G= (F11)	XP_005262878.1:n.*622G=
XM_005262822.2:c.*622G= (F11)	XP_005262879.1:n.*622G=
XM_005262823.2:c.*622G= (F11)	XP_005262880.1:n.*622G=
XM_006714137.1:c.*622G= (F11)	XP_006714200.1:n.*622G=
XM_005262821.4:c.*622G= (F11)	XP_005262878.1:n.*622G=
XM_005262822.4:c.*622G= (F11)	XP_005262879.1:n.*622G=
XM_005262823.4:c.*622G= (F11)	XP_005262880.1:n.*622G=
XM_006714137.3:c.*622G= (F11)	XP_006714200.1:n.*622G=
NM_000128.4:c.*622G= (F11) MANE Select	NP_000119.1:n.*622G=