Canonical Allele Identifier: CA358941942

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205338C>A (hg19) ; chr4:g.186284184C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284184C>A , CM000666.2:g.186284184C>A	GRCh38
NC_000004.11:g.187205338C>A , CM000666.1:g.187205338C>A	GRCh37
NC_000004.10:g.187442332C>A	NCBI36
NG_008051.1:g.23221C>A , LRG_583:g.23221C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1228C>A MANE Select	ENSP00000384957.2:p.Pro410Thr
ENST00000264692.8:c.1066C>A	ENSP00000264692.5:p.Pro356Thr
ENST00000403665.6:c.1228C>A	ENSP00000384957.2:p.Pro410Thr
NM_000128.3:c.1228C>A , LRG_583t1:c.1228C>A	NP_000119.1:p.Pro410Thr
XM_005262821.2:c.1231C>A	XP_005262878.1:p.Pro411Thr
XM_005262822.2:c.1231C>A	XP_005262879.1:p.Pro411Thr
XM_005262823.2:c.961C>A	XP_005262880.1:p.Pro321Thr
XM_005262824.1:c.1231C>A	XP_005262881.1:p.Pro411Thr
XM_006714137.1:c.1183C>A	XP_006714200.1:p.Pro395Thr
XR_938706.1:n.1636C>A
XR_938707.1:n.1636C>A
XM_005262821.4:c.1231C>A	XP_005262878.1:p.Pro411Thr
XM_005262822.4:c.1231C>A	XP_005262879.1:p.Pro411Thr
XM_005262823.4:c.961C>A	XP_005262880.1:p.Pro321Thr
XM_006714137.3:c.1183C>A	XP_006714200.1:p.Pro395Thr
XM_017007884.2:c.*2200C>A	XP_016863373.1:n.*2200C>A
XR_001741172.2:n.1702C>A
NM_000128.4:c.1228C>A MANE Select	NP_000119.1:p.Pro410Thr