Canonical Allele Identifier: CA442638880

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205256C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284102C>A , CM000666.2:g.186284102C>A	GRCh38
NC_000004.11:g.187205256C>A , CM000666.1:g.187205256C>A	GRCh37
NC_000004.10:g.187442250C>A	NCBI36
NG_008051.1:g.23139C>A , LRG_583:g.23139C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1146C>A MANE Select	ENSP00000384957.2:p.Thr382=
ENST00000264692.8:c.984C>A	ENSP00000264692.5:p.Thr328=
ENST00000403665.6:c.1146C>A	ENSP00000384957.2:p.Thr382=
NM_000128.3:c.1146C>A , LRG_583t1:c.1146C>A	NP_000119.1:p.Thr382=
XM_005262821.2:c.1149C>A	XP_005262878.1:p.Thr383=
XM_005262822.2:c.1149C>A	XP_005262879.1:p.Thr383=
XM_005262823.2:c.879C>A	XP_005262880.1:p.Thr293=
XM_005262824.1:c.1149C>A	XP_005262881.1:p.Thr383=
XM_006714137.1:c.1101C>A	XP_006714200.1:p.Thr367=
XR_938706.1:n.1554C>A
XR_938707.1:n.1554C>A
XM_005262821.4:c.1149C>A	XP_005262878.1:p.Thr383=
XM_005262822.4:c.1149C>A	XP_005262879.1:p.Thr383=
XM_005262823.4:c.879C>A	XP_005262880.1:p.Thr293=
XM_006714137.3:c.1101C>A	XP_006714200.1:p.Thr367=
XM_017007884.2:c.*2118C>A	XP_016863373.1:n.*2118C>A
XM_017007885.2:c.*14C>A	XP_016863374.1:n.*14C>A
XR_001741172.2:n.1620C>A
NM_000128.4:c.1146C>A MANE Select	NP_000119.1:p.Thr382=