Canonical Allele Identifier: CA442641628

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209818G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288664G>C , CM000666.2:g.186288664G>C	GRCh38
NC_000004.11:g.187209818G>C , CM000666.1:g.187209818G>C	GRCh37
NC_000004.10:g.187446812G>C	NCBI36
NG_008051.1:g.27701G>C , LRG_583:g.27701G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*50G>C (F11) MANE Select	ENSP00000384957.2:n.*50G>C
ENST00000264691.4:c.528G>C (F11)
ENST00000264692.8:c.*50G>C (F11)	ENSP00000264692.5:n.*50G>C
ENST00000403665.6:c.*50G>C (F11)	ENSP00000384957.2:n.*50G>C
ENST00000503841.1:n.447G>C (F11)
NM_000128.3:c.*50G>C , LRG_583t1:c.*50G>C (F11)	NP_000119.1:n.*50G>C
NR_033900.1:n.830C>G (F11-AS1)
XM_005262821.2:c.*50G>C (F11)	XP_005262878.1:n.*50G>C
XM_005262822.2:c.*50G>C (F11)	XP_005262879.1:n.*50G>C
XM_005262823.2:c.*50G>C (F11)	XP_005262880.1:n.*50G>C
XM_006714137.1:c.*50G>C (F11)	XP_006714200.1:n.*50G>C
XM_005262821.4:c.*50G>C (F11)	XP_005262878.1:n.*50G>C
XM_005262822.4:c.*50G>C (F11)	XP_005262879.1:n.*50G>C
XM_005262823.4:c.*50G>C (F11)	XP_005262880.1:n.*50G>C
XM_006714137.3:c.*50G>C (F11)	XP_006714200.1:n.*50G>C
NM_000128.4:c.*50G>C (F11) MANE Select	NP_000119.1:n.*50G>C