Canonical Allele Identifier: CA442638936

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205283A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284129A>G , CM000666.2:g.186284129A>G	GRCh38
NC_000004.11:g.187205283A>G , CM000666.1:g.187205283A>G	GRCh37
NC_000004.10:g.187442277A>G	NCBI36
NG_008051.1:g.23166A>G , LRG_583:g.23166A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1173A>G MANE Select	ENSP00000384957.2:p.Gly391=
ENST00000264692.8:c.1011A>G	ENSP00000264692.5:p.Gly337=
ENST00000403665.6:c.1173A>G	ENSP00000384957.2:p.Gly391=
NM_000128.3:c.1173A>G , LRG_583t1:c.1173A>G	NP_000119.1:p.Gly391=
XM_005262821.2:c.1176A>G	XP_005262878.1:p.Gly392=
XM_005262822.2:c.1176A>G	XP_005262879.1:p.Gly392=
XM_005262823.2:c.906A>G	XP_005262880.1:p.Gly302=
XM_005262824.1:c.1176A>G	XP_005262881.1:p.Gly392=
XM_006714137.1:c.1128A>G	XP_006714200.1:p.Gly376=
XR_938706.1:n.1581A>G
XR_938707.1:n.1581A>G
XM_005262821.4:c.1176A>G	XP_005262878.1:p.Gly392=
XM_005262822.4:c.1176A>G	XP_005262879.1:p.Gly392=
XM_005262823.4:c.906A>G	XP_005262880.1:p.Gly302=
XM_006714137.3:c.1128A>G	XP_006714200.1:p.Gly376=
XM_017007884.2:c.*2145A>G	XP_016863373.1:n.*2145A>G
XM_017007885.2:c.*41A>G	XP_016863374.1:n.*41A>G
XR_001741172.2:n.1647A>G
NM_000128.4:c.1173A>G MANE Select	NP_000119.1:p.Gly391=