Canonical Allele Identifier: CA442642353

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1240546155
• gnomAD v4: 4-186288875-C-T
• MyVariant Identifiers: chr4:g.187210029C>T (hg19) ; chr4:g.186288875C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288875C>T , CM000666.2:g.186288875C>T	GRCh38
NC_000004.11:g.187210029C>T , CM000666.1:g.187210029C>T	GRCh37
NC_000004.10:g.187447023C>T	NCBI36
NG_008051.1:g.27912C>T , LRG_583:g.27912C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*261C>T (F11) MANE Select	ENSP00000384957.2:n.*261C>T
NM_000128.3:c.*261C>T , LRG_583t1:c.*261C>T (F11)	NP_000119.1:n.*261C>T
NR_033900.1:n.619G>A (F11-AS1)
XM_005262821.2:c.*261C>T (F11)	XP_005262878.1:n.*261C>T
XM_005262822.2:c.*261C>T (F11)	XP_005262879.1:n.*261C>T
XM_005262823.2:c.*261C>T (F11)	XP_005262880.1:n.*261C>T
XM_006714137.1:c.*261C>T (F11)	XP_006714200.1:n.*261C>T
XM_005262821.4:c.*261C>T (F11)	XP_005262878.1:n.*261C>T
XM_005262822.4:c.*261C>T (F11)	XP_005262879.1:n.*261C>T
XM_005262823.4:c.*261C>T (F11)	XP_005262880.1:n.*261C>T
XM_006714137.3:c.*261C>T (F11)	XP_006714200.1:n.*261C>T
NM_000128.4:c.*261C>T (F11) MANE Select	NP_000119.1:n.*261C>T