Canonical Allele Identifier: CA442884020

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187201513A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280359A>T , CM000666.2:g.186280359A>T	GRCh38
NC_000004.11:g.187201513A>T , CM000666.1:g.187201513A>T	GRCh37
NC_000004.10:g.187438507A>T	NCBI36
NG_008051.1:g.19396A>T , LRG_583:g.19396A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1002A>T MANE Select	ENSP00000384957.2:p.Pro334=
ENST00000264692.8:c.840A>T	ENSP00000264692.5:p.Pro280=
ENST00000403665.6:c.1002A>T	ENSP00000384957.2:p.Pro334=
ENST00000452239.1:c.449A>T
NM_000128.3:c.1002A>T , LRG_583t1:c.1002A>T	NP_000119.1:p.Pro334=
XM_005262821.2:c.1002A>T	XP_005262878.1:p.Pro334=
XM_005262822.2:c.1002A>T	XP_005262879.1:p.Pro334=
XM_005262823.2:c.732A>T	XP_005262880.1:p.Pro244=
XM_005262824.1:c.1002A>T	XP_005262881.1:p.Pro334=
XM_006714137.1:c.954A>T	XP_006714200.1:p.Pro318=
XR_938706.1:n.1354A>T
XR_938707.1:n.1354A>T
XM_005262821.4:c.1002A>T	XP_005262878.1:p.Pro334=
XM_005262822.4:c.1002A>T	XP_005262879.1:p.Pro334=
XM_005262823.4:c.732A>T	XP_005262880.1:p.Pro244=
XM_006714137.3:c.954A>T	XP_006714200.1:p.Pro318=
XM_017007884.2:c.1002A>T	XP_016863373.1:p.Pro334=
XM_017007885.2:c.1002A>T	XP_016863374.1:p.Pro334=
XM_017007886.2:c.1002A>T	XP_016863375.1:p.Pro334=
XR_001741172.2:n.1335A>T
NM_000128.4:c.1002A>T MANE Select	NP_000119.1:p.Pro334=