Canonical Allele Identifier: CA358941794

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205307G>A (hg19) ; chr4:g.186284153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284153G>A , CM000666.2:g.186284153G>A	GRCh38
NC_000004.11:g.187205307G>A , CM000666.1:g.187205307G>A	GRCh37
NC_000004.10:g.187442301G>A	NCBI36
NG_008051.1:g.23190G>A , LRG_583:g.23190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1197G>A MANE Select	ENSP00000384957.2:p.Trp399Ter
ENST00000264692.8:c.1035G>A	ENSP00000264692.5:p.Trp345Ter
ENST00000403665.6:c.1197G>A	ENSP00000384957.2:p.Trp399Ter
NM_000128.3:c.1197G>A , LRG_583t1:c.1197G>A	NP_000119.1:p.Trp399Ter
XM_005262821.2:c.1200G>A	XP_005262878.1:p.Trp400Ter
XM_005262822.2:c.1200G>A	XP_005262879.1:p.Trp400Ter
XM_005262823.2:c.930G>A	XP_005262880.1:p.Trp310Ter
XM_005262824.1:c.1200G>A	XP_005262881.1:p.Trp400Ter
XM_006714137.1:c.1152G>A	XP_006714200.1:p.Trp384Ter
XR_938706.1:n.1605G>A
XR_938707.1:n.1605G>A
XM_005262821.4:c.1200G>A	XP_005262878.1:p.Trp400Ter
XM_005262822.4:c.1200G>A	XP_005262879.1:p.Trp400Ter
XM_005262823.4:c.930G>A	XP_005262880.1:p.Trp310Ter
XM_006714137.3:c.1152G>A	XP_006714200.1:p.Trp384Ter
XM_017007884.2:c.*2169G>A	XP_016863373.1:n.*2169G>A
XM_017007885.2:c.*65G>A	XP_016863374.1:n.*65G>A
XR_001741172.2:n.1671G>A
NM_000128.4:c.1197G>A MANE Select	NP_000119.1:p.Trp399Ter