Canonical Allele Identifier: CA442638989

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205310G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284156G>C , CM000666.2:g.186284156G>C	GRCh38
NC_000004.11:g.187205310G>C , CM000666.1:g.187205310G>C	GRCh37
NC_000004.10:g.187442304G>C	NCBI36
NG_008051.1:g.23193G>C , LRG_583:g.23193G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1200G>C MANE Select	ENSP00000384957.2:p.Pro400=
ENST00000264692.8:c.1038G>C	ENSP00000264692.5:p.Pro346=
ENST00000403665.6:c.1200G>C	ENSP00000384957.2:p.Pro400=
NM_000128.3:c.1200G>C , LRG_583t1:c.1200G>C	NP_000119.1:p.Pro400=
XM_005262821.2:c.1203G>C	XP_005262878.1:p.Pro401=
XM_005262822.2:c.1203G>C	XP_005262879.1:p.Pro401=
XM_005262823.2:c.933G>C	XP_005262880.1:p.Pro311=
XM_005262824.1:c.1203G>C	XP_005262881.1:p.Pro401=
XM_006714137.1:c.1155G>C	XP_006714200.1:p.Pro385=
XR_938706.1:n.1608G>C
XR_938707.1:n.1608G>C
XM_005262821.4:c.1203G>C	XP_005262878.1:p.Pro401=
XM_005262822.4:c.1203G>C	XP_005262879.1:p.Pro401=
XM_005262823.4:c.933G>C	XP_005262880.1:p.Pro311=
XM_006714137.3:c.1155G>C	XP_006714200.1:p.Pro385=
XM_017007884.2:c.*2172G>C	XP_016863373.1:n.*2172G>C
XM_017007885.2:c.*68G>C	XP_016863374.1:n.*68G>C
XR_001741172.2:n.1674G>C
NM_000128.4:c.1200G>C MANE Select	NP_000119.1:p.Pro400=