Canonical Allele Identifier: CA358941878

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205323C>G (hg19) ; chr4:g.186284169C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284169C>G , CM000666.2:g.186284169C>G	GRCh38
NC_000004.11:g.187205323C>G , CM000666.1:g.187205323C>G	GRCh37
NC_000004.10:g.187442317C>G	NCBI36
NG_008051.1:g.23206C>G , LRG_583:g.23206C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1213C>G MANE Select	ENSP00000384957.2:p.Leu405Val
ENST00000264692.8:c.1051C>G	ENSP00000264692.5:p.Leu351Val
ENST00000403665.6:c.1213C>G	ENSP00000384957.2:p.Leu405Val
NM_000128.3:c.1213C>G , LRG_583t1:c.1213C>G	NP_000119.1:p.Leu405Val
XM_005262821.2:c.1216C>G	XP_005262878.1:p.Leu406Val
XM_005262822.2:c.1216C>G	XP_005262879.1:p.Leu406Val
XM_005262823.2:c.946C>G	XP_005262880.1:p.Leu316Val
XM_005262824.1:c.1216C>G	XP_005262881.1:p.Leu406Val
XM_006714137.1:c.1168C>G	XP_006714200.1:p.Leu390Val
XR_938706.1:n.1621C>G
XR_938707.1:n.1621C>G
XM_005262821.4:c.1216C>G	XP_005262878.1:p.Leu406Val
XM_005262822.4:c.1216C>G	XP_005262879.1:p.Leu406Val
XM_005262823.4:c.946C>G	XP_005262880.1:p.Leu316Val
XM_006714137.3:c.1168C>G	XP_006714200.1:p.Leu390Val
XM_017007884.2:c.*2185C>G	XP_016863373.1:n.*2185C>G
XR_001741172.2:n.1687C>G
NM_000128.4:c.1213C>G MANE Select	NP_000119.1:p.Leu405Val