Canonical Allele Identifier: CA358941494

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205249G>T (hg19) ; chr4:g.186284095G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284095G>T , CM000666.2:g.186284095G>T	GRCh38
NC_000004.11:g.187205249G>T , CM000666.1:g.187205249G>T	GRCh37
NC_000004.10:g.187442243G>T	NCBI36
NG_008051.1:g.23132G>T , LRG_583:g.23132G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1139G>T MANE Select	ENSP00000384957.2:p.Cys380Phe
ENST00000264692.8:c.977G>T	ENSP00000264692.5:p.Cys326Phe
ENST00000403665.6:c.1139G>T	ENSP00000384957.2:p.Cys380Phe
NM_000128.3:c.1139G>T , LRG_583t1:c.1139G>T	NP_000119.1:p.Cys380Phe
XM_005262821.2:c.1142G>T	XP_005262878.1:p.Cys381Phe
XM_005262822.2:c.1142G>T	XP_005262879.1:p.Cys381Phe
XM_005262823.2:c.872G>T	XP_005262880.1:p.Cys291Phe
XM_005262824.1:c.1142G>T	XP_005262881.1:p.Cys381Phe
XM_006714137.1:c.1094G>T	XP_006714200.1:p.Cys365Phe
XR_938706.1:n.1547G>T
XR_938707.1:n.1547G>T
XM_005262821.4:c.1142G>T	XP_005262878.1:p.Cys381Phe
XM_005262822.4:c.1142G>T	XP_005262879.1:p.Cys381Phe
XM_005262823.4:c.872G>T	XP_005262880.1:p.Cys291Phe
XM_006714137.3:c.1094G>T	XP_006714200.1:p.Cys365Phe
XM_017007884.2:c.*2111G>T	XP_016863373.1:n.*2111G>T
XM_017007885.2:c.*7G>T	XP_016863374.1:n.*7G>T
XR_001741172.2:n.1613G>T
NM_000128.4:c.1139G>T MANE Select	NP_000119.1:p.Cys380Phe