Canonical Allele Identifier: CA358938760

Gene: F11

Linked Data

• gnomAD v4: 4-186280514-A-C
• MyVariant Identifiers: chr4:g.187201668A>C (hg19) ; chr4:g.186280514A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186280514A>C , CM000666.2:g.186280514A>C	GRCh38
NC_000004.11:g.187201668A>C , CM000666.1:g.187201668A>C	GRCh37
NC_000004.10:g.187438662A>C	NCBI36
NG_008051.1:g.19551A>C , LRG_583:g.19551A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1069A>C MANE Select	ENSP00000384957.2:p.Thr357Pro
ENST00000264692.8:c.907A>C	ENSP00000264692.5:p.Thr303Pro
ENST00000403665.6:c.1069A>C	ENSP00000384957.2:p.Thr357Pro
ENST00000452239.1:c.516A>C
NM_000128.3:c.1069A>C , LRG_583t1:c.1069A>C	NP_000119.1:p.Thr357Pro
XM_005262821.2:c.1072A>C	XP_005262878.1:p.Thr358Pro
XM_005262822.2:c.1072A>C	XP_005262879.1:p.Thr358Pro
XM_005262823.2:c.802A>C	XP_005262880.1:p.Thr268Pro
XM_005262824.1:c.1072A>C	XP_005262881.1:p.Thr358Pro
XM_006714137.1:c.1024A>C	XP_006714200.1:p.Thr342Pro
XR_938706.1:n.1424A>C
XR_938707.1:n.1424A>C
XM_005262821.4:c.1072A>C	XP_005262878.1:p.Thr358Pro
XM_005262822.4:c.1072A>C	XP_005262879.1:p.Thr358Pro
XM_005262823.4:c.802A>C	XP_005262880.1:p.Thr268Pro
XM_006714137.3:c.1024A>C	XP_006714200.1:p.Thr342Pro
XM_017007884.2:c.1072A>C	XP_016863373.1:p.Thr358Pro
XM_017007885.2:c.1072A>C	XP_016863374.1:p.Thr358Pro
XM_017007886.2:c.1069A>C	XP_016863375.1:p.Thr357Pro
XR_001741172.2:n.1490A>C
NM_000128.4:c.1069A>C MANE Select	NP_000119.1:p.Thr357Pro