Canonical Allele Identifier: CA442641363

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209654T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288500T>C , CM000666.2:g.186288500T>C	GRCh38
NC_000004.11:g.187209654T>C , CM000666.1:g.187209654T>C	GRCh37
NC_000004.10:g.187446648T>C	NCBI36
NG_008051.1:g.27537T>C , LRG_583:g.27537T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1764T>C (F11) MANE Select	ENSP00000384957.2:p.His588=
ENST00000264691.4:c.364T>C (F11)
ENST00000264692.8:c.1602T>C (F11)	ENSP00000264692.5:p.His534=
ENST00000403665.6:c.1764T>C (F11)	ENSP00000384957.2:p.His588=
ENST00000503841.1:n.283T>C (F11)
NM_000128.3:c.1764T>C , LRG_583t1:c.1764T>C (F11)	NP_000119.1:p.His588=
NR_033900.1:n.994A>G (F11-AS1)
XM_005262821.2:c.1767T>C (F11)	XP_005262878.1:p.His589=
XM_005262822.2:c.1671T>C (F11)	XP_005262879.1:p.His557=
XM_005262823.2:c.1497T>C (F11)	XP_005262880.1:p.His499=
XM_006714137.1:c.1719T>C (F11)	XP_006714200.1:p.His573=
XM_005262821.4:c.1767T>C (F11)	XP_005262878.1:p.His589=
XM_005262822.4:c.1671T>C (F11)	XP_005262879.1:p.His557=
XM_005262823.4:c.1497T>C (F11)	XP_005262880.1:p.His499=
XM_006714137.3:c.1719T>C (F11)	XP_006714200.1:p.His573=
NM_000128.4:c.1764T>C (F11) MANE Select	NP_000119.1:p.His588=