Canonical Allele Identifier: CA442641409

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209726C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288572C>G , CM000666.2:g.186288572C>G	GRCh38
NC_000004.11:g.187209726C>G , CM000666.1:g.187209726C>G	GRCh37
NC_000004.10:g.187446720C>G	NCBI36
NG_008051.1:g.27609C>G , LRG_583:g.27609C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1836C>G (F11) MANE Select	ENSP00000384957.2:p.Val612=
ENST00000264691.4:c.436C>G (F11)
ENST00000264692.8:c.1674C>G (F11)	ENSP00000264692.5:p.Val558=
ENST00000403665.6:c.1836C>G (F11)	ENSP00000384957.2:p.Val612=
ENST00000503841.1:n.355C>G (F11)
NM_000128.3:c.1836C>G , LRG_583t1:c.1836C>G (F11)	NP_000119.1:p.Val612=
NR_033900.1:n.922G>C (F11-AS1)
XM_005262821.2:c.1839C>G (F11)	XP_005262878.1:p.Val613=
XM_005262822.2:c.1743C>G (F11)	XP_005262879.1:p.Val581=
XM_005262823.2:c.1569C>G (F11)	XP_005262880.1:p.Val523=
XM_006714137.1:c.1791C>G (F11)	XP_006714200.1:p.Val597=
XM_005262821.4:c.1839C>G (F11)	XP_005262878.1:p.Val613=
XM_005262822.4:c.1743C>G (F11)	XP_005262879.1:p.Val581=
XM_005262823.4:c.1569C>G (F11)	XP_005262880.1:p.Val523=
XM_006714137.3:c.1791C>G (F11)	XP_006714200.1:p.Val597=
NM_000128.4:c.1836C>G (F11) MANE Select	NP_000119.1:p.Val612=