Canonical Allele Identifier: CA442641379

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209678C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288524C>G , CM000666.2:g.186288524C>G	GRCh38
NC_000004.11:g.187209678C>G , CM000666.1:g.187209678C>G	GRCh37
NC_000004.10:g.187446672C>G	NCBI36
NG_008051.1:g.27561C>G , LRG_583:g.27561C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1788C>G (F11) MANE Select	ENSP00000384957.2:p.Gly596=
ENST00000264691.4:c.388C>G (F11)
ENST00000264692.8:c.1626C>G (F11)	ENSP00000264692.5:p.Gly542=
ENST00000403665.6:c.1788C>G (F11)	ENSP00000384957.2:p.Gly596=
ENST00000503841.1:n.307C>G (F11)
NM_000128.3:c.1788C>G , LRG_583t1:c.1788C>G (F11)	NP_000119.1:p.Gly596=
NR_033900.1:n.970G>C (F11-AS1)
XM_005262821.2:c.1791C>G (F11)	XP_005262878.1:p.Gly597=
XM_005262822.2:c.1695C>G (F11)	XP_005262879.1:p.Gly565=
XM_005262823.2:c.1521C>G (F11)	XP_005262880.1:p.Gly507=
XM_006714137.1:c.1743C>G (F11)	XP_006714200.1:p.Gly581=
XM_005262821.4:c.1791C>G (F11)	XP_005262878.1:p.Gly597=
XM_005262822.4:c.1695C>G (F11)	XP_005262879.1:p.Gly565=
XM_005262823.4:c.1521C>G (F11)	XP_005262880.1:p.Gly507=
XM_006714137.3:c.1743C>G (F11)	XP_006714200.1:p.Gly581=
NM_000128.4:c.1788C>G (F11) MANE Select	NP_000119.1:p.Gly596=