Canonical Allele Identifier: CA442641434

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209756T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288602T>C , CM000666.2:g.186288602T>C	GRCh38
NC_000004.11:g.187209756T>C , CM000666.1:g.187209756T>C	GRCh37
NC_000004.10:g.187446750T>C	NCBI36
NG_008051.1:g.27639T>C , LRG_583:g.27639T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1866T>C (F11) MANE Select	ENSP00000384957.2:p.Thr622=
ENST00000264691.4:c.466T>C (F11)
ENST00000264692.8:c.1704T>C (F11)	ENSP00000264692.5:p.Thr568=
ENST00000403665.6:c.1866T>C (F11)	ENSP00000384957.2:p.Thr622=
ENST00000503841.1:n.385T>C (F11)
NM_000128.3:c.1866T>C , LRG_583t1:c.1866T>C (F11)	NP_000119.1:p.Thr622=
NR_033900.1:n.892A>G (F11-AS1)
XM_005262821.2:c.1869T>C (F11)	XP_005262878.1:p.Thr623=
XM_005262822.2:c.1773T>C (F11)	XP_005262879.1:p.Thr591=
XM_005262823.2:c.1599T>C (F11)	XP_005262880.1:p.Thr533=
XM_006714137.1:c.1821T>C (F11)	XP_006714200.1:p.Thr607=
XM_005262821.4:c.1869T>C (F11)	XP_005262878.1:p.Thr623=
XM_005262822.4:c.1773T>C (F11)	XP_005262879.1:p.Thr591=
XM_005262823.4:c.1599T>C (F11)	XP_005262880.1:p.Thr533=
XM_006714137.3:c.1821T>C (F11)	XP_006714200.1:p.Thr607=
NM_000128.4:c.1866T>C (F11) MANE Select	NP_000119.1:p.Thr622=