Canonical Allele Identifier: CA442638903

Gene: F11

Linked Data

• gnomAD v4: 4-186284114-C-T
• COSMIC: COSM3917565 ; COSM3917566
• MyVariant Identifiers: chr4:g.187205268C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284114C>T , CM000666.2:g.186284114C>T	GRCh38
NC_000004.11:g.187205268C>T , CM000666.1:g.187205268C>T	GRCh37
NC_000004.10:g.187442262C>T	NCBI36
NG_008051.1:g.23151C>T , LRG_583:g.23151C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1158C>T MANE Select	ENSP00000384957.2:p.Pro386=
ENST00000264692.8:c.996C>T	ENSP00000264692.5:p.Pro332=
ENST00000403665.6:c.1158C>T	ENSP00000384957.2:p.Pro386=
NM_000128.3:c.1158C>T , LRG_583t1:c.1158C>T	NP_000119.1:p.Pro386=
XM_005262821.2:c.1161C>T	XP_005262878.1:p.Pro387=
XM_005262822.2:c.1161C>T	XP_005262879.1:p.Pro387=
XM_005262823.2:c.891C>T	XP_005262880.1:p.Pro297=
XM_005262824.1:c.1161C>T	XP_005262881.1:p.Pro387=
XM_006714137.1:c.1113C>T	XP_006714200.1:p.Pro371=
XR_938706.1:n.1566C>T
XR_938707.1:n.1566C>T
XM_005262821.4:c.1161C>T	XP_005262878.1:p.Pro387=
XM_005262822.4:c.1161C>T	XP_005262879.1:p.Pro387=
XM_005262823.4:c.891C>T	XP_005262880.1:p.Pro297=
XM_006714137.3:c.1113C>T	XP_006714200.1:p.Pro371=
XM_017007884.2:c.*2130C>T	XP_016863373.1:n.*2130C>T
XM_017007885.2:c.*26C>T	XP_016863374.1:n.*26C>T
XR_001741172.2:n.1632C>T
NM_000128.4:c.1158C>T MANE Select	NP_000119.1:p.Pro386=