Canonical Allele Identifier: CA3163971

Gene: F11

Linked Data

• dbSNP Id: rs754649628
• ExAC: 4:187206861 A / C
• gnomAD v2: 4-187206861-A-C
• gnomAD v4: 4-186285707-A-C
• MyVariant Identifiers: chr4:g.187206861A>C (hg19) ; chr4:g.186285707A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285707A>C , CM000666.2:g.186285707A>C	GRCh38
NC_000004.11:g.187206861A>C , CM000666.1:g.187206861A>C	GRCh37
NC_000004.10:g.187443855A>C	NCBI36
NG_008051.1:g.24744A>C , LRG_583:g.24744A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1374A>C MANE Select	ENSP00000384957.2:p.Thr458=
ENST00000264691.4:c.70A>C
ENST00000264692.8:c.1212A>C	ENSP00000264692.5:p.Thr404=
ENST00000403665.6:c.1374A>C	ENSP00000384957.2:p.Thr458=
NM_000128.3:c.1374A>C , LRG_583t1:c.1374A>C	NP_000119.1:p.Thr458=
XM_005262821.2:c.1377A>C	XP_005262878.1:p.Thr459=
XM_005262822.2:c.1377A>C	XP_005262879.1:p.Thr459=
XM_005262823.2:c.1107A>C	XP_005262880.1:p.Thr369=
XM_005262824.1:c.1377A>C	XP_005262881.1:p.Thr459=
XM_006714137.1:c.1329A>C	XP_006714200.1:p.Thr443=
XR_938706.1:n.1782A>C
XR_938707.1:n.1782A>C
XM_005262821.4:c.1377A>C	XP_005262878.1:p.Thr459=
XM_005262822.4:c.1377A>C	XP_005262879.1:p.Thr459=
XM_005262823.4:c.1107A>C	XP_005262880.1:p.Thr369=
XM_006714137.3:c.1329A>C	XP_006714200.1:p.Thr443=
XR_001741172.2:n.1848A>C
NM_000128.4:c.1374A>C MANE Select	NP_000119.1:p.Thr458=