Canonical Allele Identifier: CA442639253

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187206831T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285677T>C , CM000666.2:g.186285677T>C	GRCh38
NC_000004.11:g.187206831T>C , CM000666.1:g.187206831T>C	GRCh37
NC_000004.10:g.187443825T>C	NCBI36
NG_008051.1:g.24714T>C , LRG_583:g.24714T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1344T>C MANE Select	ENSP00000384957.2:p.Ile448=
ENST00000264691.4:c.40T>C
ENST00000264692.8:c.1182T>C	ENSP00000264692.5:p.Ile394=
ENST00000403665.6:c.1344T>C	ENSP00000384957.2:p.Ile448=
NM_000128.3:c.1344T>C , LRG_583t1:c.1344T>C	NP_000119.1:p.Ile448=
XM_005262821.2:c.1347T>C	XP_005262878.1:p.Ile449=
XM_005262822.2:c.1347T>C	XP_005262879.1:p.Ile449=
XM_005262823.2:c.1077T>C	XP_005262880.1:p.Ile359=
XM_005262824.1:c.1347T>C	XP_005262881.1:p.Ile449=
XM_006714137.1:c.1299T>C	XP_006714200.1:p.Ile433=
XR_938706.1:n.1752T>C
XR_938707.1:n.1752T>C
XM_005262821.4:c.1347T>C	XP_005262878.1:p.Ile449=
XM_005262822.4:c.1347T>C	XP_005262879.1:p.Ile449=
XM_005262823.4:c.1077T>C	XP_005262880.1:p.Ile359=
XM_006714137.3:c.1299T>C	XP_006714200.1:p.Ile433=
XR_001741172.2:n.1818T>C
NM_000128.4:c.1344T>C MANE Select	NP_000119.1:p.Ile448=