Canonical Allele Identifier: CA442639039

Gene: F11

Linked Data

• dbSNP Id: rs1741004090
• MyVariant Identifiers: chr4:g.187205331A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284177A>C , CM000666.2:g.186284177A>C	GRCh38
NC_000004.11:g.187205331A>C , CM000666.1:g.187205331A>C	GRCh37
NC_000004.10:g.187442325A>C	NCBI36
NG_008051.1:g.23214A>C , LRG_583:g.23214A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1221A>C MANE Select	ENSP00000384957.2:p.Thr407=
ENST00000264692.8:c.1059A>C	ENSP00000264692.5:p.Thr353=
ENST00000403665.6:c.1221A>C	ENSP00000384957.2:p.Thr407=
NM_000128.3:c.1221A>C , LRG_583t1:c.1221A>C	NP_000119.1:p.Thr407=
XM_005262821.2:c.1224A>C	XP_005262878.1:p.Thr408=
XM_005262822.2:c.1224A>C	XP_005262879.1:p.Thr408=
XM_005262823.2:c.954A>C	XP_005262880.1:p.Thr318=
XM_005262824.1:c.1224A>C	XP_005262881.1:p.Thr408=
XM_006714137.1:c.1176A>C	XP_006714200.1:p.Thr392=
XR_938706.1:n.1629A>C
XR_938707.1:n.1629A>C
XM_005262821.4:c.1224A>C	XP_005262878.1:p.Thr408=
XM_005262822.4:c.1224A>C	XP_005262879.1:p.Thr408=
XM_005262823.4:c.954A>C	XP_005262880.1:p.Thr318=
XM_006714137.3:c.1176A>C	XP_006714200.1:p.Thr392=
XM_017007884.2:c.*2193A>C	XP_016863373.1:n.*2193A>C
XR_001741172.2:n.1695A>C
NM_000128.4:c.1221A>C MANE Select	NP_000119.1:p.Thr407=