Canonical Allele Identifier: CA3163915
Gene: F11 HGNC NCBI

Linked Data

ClinVar Variation Id: 255176
dbSNP Id: rs5970

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186284147T>C , CM000666.2:g.186284147T>C GRCh38
NC_000004.11:g.187205301T>C , CM000666.1:g.187205301T>C GRCh37
NC_000004.10:g.187442295T>C NCBI36
NG_008051.1:g.23184T>C , LRG_583:g.23184T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403665.7:c.1191T>C MANE Select ENSP00000384957.2:p.Gly397=
ENST00000264692.8:c.1029T>C ENSP00000264692.5:p.Gly343=
ENST00000403665.6:c.1191T>C ENSP00000384957.2:p.Gly397=
NM_000128.3:c.1191T>C , LRG_583t1:c.1191T>C NP_000119.1:p.Gly397=
XM_005262821.2:c.1194T>C XP_005262878.1:p.Gly398=
XM_005262822.2:c.1194T>C XP_005262879.1:p.Gly398=
XM_005262823.2:c.924T>C XP_005262880.1:p.Gly308=
XM_005262824.1:c.1194T>C XP_005262881.1:p.Gly398=
XM_006714137.1:c.1146T>C XP_006714200.1:p.Gly382=
XR_938706.1:n.1599T>C
XR_938707.1:n.1599T>C
XM_005262821.4:c.1194T>C XP_005262878.1:p.Gly398=
XM_005262822.4:c.1194T>C XP_005262879.1:p.Gly398=
XM_005262823.4:c.924T>C XP_005262880.1:p.Gly308=
XM_006714137.3:c.1146T>C XP_006714200.1:p.Gly382=
XM_017007884.2:c.*2163T>C XP_016863373.1:n.*2163T>C
XM_017007885.2:c.*59T>C XP_016863374.1:n.*59T>C
XR_001741172.2:n.1665T>C
NM_000128.4:c.1191T>C MANE Select NP_000119.1:p.Gly397=