Canonical Allele Identifier: CA442884474

Gene: F11

Linked Data

• gnomAD v4: 4-186280513-A-C
• MyVariant Identifiers: chr4:g.187201667A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280513A>C , CM000666.2:g.186280513A>C	GRCh38
NC_000004.11:g.187201667A>C , CM000666.1:g.187201667A>C	GRCh37
NC_000004.10:g.187438661A>C	NCBI36
NG_008051.1:g.19550A>C , LRG_583:g.19550A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1068A>C MANE Select	ENSP00000384957.2:p.Pro356=
ENST00000264692.8:c.906A>C	ENSP00000264692.5:p.Pro302=
ENST00000403665.6:c.1068A>C	ENSP00000384957.2:p.Pro356=
ENST00000452239.1:c.515A>C
NM_000128.3:c.1068A>C , LRG_583t1:c.1068A>C	NP_000119.1:p.Pro356=
XM_005262821.2:c.1071A>C	XP_005262878.1:p.Pro357=
XM_005262822.2:c.1071A>C	XP_005262879.1:p.Pro357=
XM_005262823.2:c.801A>C	XP_005262880.1:p.Pro267=
XM_005262824.1:c.1071A>C	XP_005262881.1:p.Pro357=
XM_006714137.1:c.1023A>C	XP_006714200.1:p.Pro341=
XR_938706.1:n.1423A>C
XR_938707.1:n.1423A>C
XM_005262821.4:c.1071A>C	XP_005262878.1:p.Pro357=
XM_005262822.4:c.1071A>C	XP_005262879.1:p.Pro357=
XM_005262823.4:c.801A>C	XP_005262880.1:p.Pro267=
XM_006714137.3:c.1023A>C	XP_006714200.1:p.Pro341=
XM_017007884.2:c.1071A>C	XP_016863373.1:p.Pro357=
XM_017007885.2:c.1071A>C	XP_016863374.1:p.Pro357=
XM_017007886.2:c.1068A>C	XP_016863375.1:p.Pro356=
XR_001741172.2:n.1489A>C
NM_000128.4:c.1068A>C MANE Select	NP_000119.1:p.Pro356=