Canonical Allele Identifier: CA442642157

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209967T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288813T>A , CM000666.2:g.186288813T>A	GRCh38
NC_000004.11:g.187209967T>A , CM000666.1:g.187209967T>A	GRCh37
NC_000004.10:g.187446961T>A	NCBI36
NG_008051.1:g.27850T>A , LRG_583:g.27850T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*199T>A (F11) MANE Select	ENSP00000384957.2:n.*199T>A
NM_000128.3:c.*199T>A , LRG_583t1:c.*199T>A (F11)	NP_000119.1:n.*199T>A
NR_033900.1:n.681A>T (F11-AS1)
XM_005262821.2:c.*199T>A (F11)	XP_005262878.1:n.*199T>A
XM_005262822.2:c.*199T>A (F11)	XP_005262879.1:n.*199T>A
XM_005262823.2:c.*199T>A (F11)	XP_005262880.1:n.*199T>A
XM_006714137.1:c.*199T>A (F11)	XP_006714200.1:n.*199T>A
XM_005262821.4:c.*199T>A (F11)	XP_005262878.1:n.*199T>A
XM_005262822.4:c.*199T>A (F11)	XP_005262879.1:n.*199T>A
XM_005262823.4:c.*199T>A (F11)	XP_005262880.1:n.*199T>A
XM_006714137.3:c.*199T>A (F11)	XP_006714200.1:n.*199T>A
NM_000128.4:c.*199T>A (F11) MANE Select	NP_000119.1:n.*199T>A