Canonical Allele Identifier: CA442639004

Gene: F11

Linked Data

• ClinVar Variation Id: 1963897
• ClinVar RCV Id: RCV002716249
• MyVariant Identifiers: chr4:g.187205316G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284162G>A , CM000666.2:g.186284162G>A	GRCh38
NC_000004.11:g.187205316G>A , CM000666.1:g.187205316G>A	GRCh37
NC_000004.10:g.187442310G>A	NCBI36
NG_008051.1:g.23199G>A , LRG_583:g.23199G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1206G>A MANE Select	ENSP00000384957.2:p.Gln402=
ENST00000264692.8:c.1044G>A	ENSP00000264692.5:p.Gln348=
ENST00000403665.6:c.1206G>A	ENSP00000384957.2:p.Gln402=
NM_000128.3:c.1206G>A , LRG_583t1:c.1206G>A	NP_000119.1:p.Gln402=
XM_005262821.2:c.1209G>A	XP_005262878.1:p.Gln403=
XM_005262822.2:c.1209G>A	XP_005262879.1:p.Gln403=
XM_005262823.2:c.939G>A	XP_005262880.1:p.Gln313=
XM_005262824.1:c.1209G>A	XP_005262881.1:p.Gln403=
XM_006714137.1:c.1161G>A	XP_006714200.1:p.Gln387=
XR_938706.1:n.1614G>A
XR_938707.1:n.1614G>A
XM_005262821.4:c.1209G>A	XP_005262878.1:p.Gln403=
XM_005262822.4:c.1209G>A	XP_005262879.1:p.Gln403=
XM_005262823.4:c.939G>A	XP_005262880.1:p.Gln313=
XM_006714137.3:c.1161G>A	XP_006714200.1:p.Gln387=
XM_017007884.2:c.*2178G>A	XP_016863373.1:n.*2178G>A
XM_017007885.2:c.*74G>A	XP_016863374.1:n.*74G>A
XR_001741172.2:n.1680G>A
NM_000128.4:c.1206G>A MANE Select	NP_000119.1:p.Gln402=