Canonical Allele Identifier: CA358945730

Gene: F11 F11-AS1

Linked Data

• dbSNP Id: rs1381953469
• gnomAD v2: 4-187208966-G-C
• gnomAD v4: 4-186287812-G-C
• MyVariant Identifiers: chr4:g.187208966G>C (hg19) ; chr4:g.186287812G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287812G>C , CM000666.2:g.186287812G>C	GRCh38
NC_000004.11:g.187208966G>C , CM000666.1:g.187208966G>C	GRCh37
NC_000004.10:g.187445960G>C	NCBI36
NG_008051.1:g.26849G>C , LRG_583:g.26849G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1705G>C (F11) MANE Select	ENSP00000384957.2:p.Asp569His
ENST00000264691.4:c.305G>C (F11)
ENST00000264692.8:c.1543G>C (F11)	ENSP00000264692.5:p.Asp515His
ENST00000403665.6:c.1705G>C (F11)	ENSP00000384957.2:p.Asp569His
ENST00000503841.1:n.224G>C (F11)
NM_000128.3:c.1705G>C , LRG_583t1:c.1705G>C (F11)	NP_000119.1:p.Asp569His
NR_033900.1:n.1066+616C>G (F11-AS1)
XM_005262821.2:c.1708G>C (F11)	XP_005262878.1:p.Asp570His
XM_005262822.2:c.1612G>C (F11)	XP_005262879.1:p.Asp538His
XM_005262823.2:c.1438G>C (F11)	XP_005262880.1:p.Asp480His
XM_006714137.1:c.1660G>C (F11)	XP_006714200.1:p.Asp554His
XM_005262821.4:c.1708G>C (F11)	XP_005262878.1:p.Asp570His
XM_005262822.4:c.1612G>C (F11)	XP_005262879.1:p.Asp538His
XM_005262823.4:c.1438G>C (F11)	XP_005262880.1:p.Asp480His
XM_006714137.3:c.1660G>C (F11)	XP_006714200.1:p.Asp554His
NM_000128.4:c.1705G>C (F11) MANE Select	NP_000119.1:p.Asp569His