Canonical Allele Identifier: CA442641373

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209666C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288512C>A , CM000666.2:g.186288512C>A	GRCh38
NC_000004.11:g.187209666C>A , CM000666.1:g.187209666C>A	GRCh37
NC_000004.10:g.187446660C>A	NCBI36
NG_008051.1:g.27549C>A , LRG_583:g.27549C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1776C>A (F11) MANE Select	ENSP00000384957.2:p.Ile592=
ENST00000264691.4:c.376C>A (F11)
ENST00000264692.8:c.1614C>A (F11)	ENSP00000264692.5:p.Ile538=
ENST00000403665.6:c.1776C>A (F11)	ENSP00000384957.2:p.Ile592=
ENST00000503841.1:n.295C>A (F11)
NM_000128.3:c.1776C>A , LRG_583t1:c.1776C>A (F11)	NP_000119.1:p.Ile592=
NR_033900.1:n.982G>T (F11-AS1)
XM_005262821.2:c.1779C>A (F11)	XP_005262878.1:p.Ile593=
XM_005262822.2:c.1683C>A (F11)	XP_005262879.1:p.Ile561=
XM_005262823.2:c.1509C>A (F11)	XP_005262880.1:p.Ile503=
XM_006714137.1:c.1731C>A (F11)	XP_006714200.1:p.Ile577=
XM_005262821.4:c.1779C>A (F11)	XP_005262878.1:p.Ile593=
XM_005262822.4:c.1683C>A (F11)	XP_005262879.1:p.Ile561=
XM_005262823.4:c.1509C>A (F11)	XP_005262880.1:p.Ile503=
XM_006714137.3:c.1731C>A (F11)	XP_006714200.1:p.Ile577=
NM_000128.4:c.1776C>A (F11) MANE Select	NP_000119.1:p.Ile592=