Canonical Allele Identifier: CA112103671

Gene: F11

Linked Data

• dbSNP Id: rs201882589
• MyVariant Identifiers: chr4:g.187206811T>G (hg19) ; chr4:g.186285657T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285657T>G , CM000666.2:g.186285657T>G	GRCh38
NC_000004.11:g.187206811T>G , CM000666.1:g.187206811T>G	GRCh37
NC_000004.10:g.187443805T>G	NCBI36
NG_008051.1:g.24694T>G , LRG_583:g.24694T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1324T>G MANE Select	ENSP00000384957.2:p.Leu442Val
ENST00000264691.4:c.20T>G
ENST00000264692.8:c.1162T>G	ENSP00000264692.5:p.Leu388Val
ENST00000403665.6:c.1324T>G	ENSP00000384957.2:p.Leu442Val
NM_000128.3:c.1324T>G , LRG_583t1:c.1324T>G	NP_000119.1:p.Leu442Val
XM_005262821.2:c.1327T>G	XP_005262878.1:p.Leu443Val
XM_005262822.2:c.1327T>G	XP_005262879.1:p.Leu443Val
XM_005262823.2:c.1057T>G	XP_005262880.1:p.Leu353Val
XM_005262824.1:c.1327T>G	XP_005262881.1:p.Leu443Val
XM_006714137.1:c.1279T>G	XP_006714200.1:p.Leu427Val
XR_938706.1:n.1732T>G
XR_938707.1:n.1732T>G
XM_005262821.4:c.1327T>G	XP_005262878.1:p.Leu443Val
XM_005262822.4:c.1327T>G	XP_005262879.1:p.Leu443Val
XM_005262823.4:c.1057T>G	XP_005262880.1:p.Leu353Val
XM_006714137.3:c.1279T>G	XP_006714200.1:p.Leu427Val
XR_001741172.2:n.1798T>G
NM_000128.4:c.1324T>G MANE Select	NP_000119.1:p.Leu442Val