Canonical Allele Identifier: CA358941888

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205326C>G (hg19) ; chr4:g.186284172C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284172C>G , CM000666.2:g.186284172C>G	GRCh38
NC_000004.11:g.187205326C>G , CM000666.1:g.187205326C>G	GRCh37
NC_000004.10:g.187442320C>G	NCBI36
NG_008051.1:g.23209C>G , LRG_583:g.23209C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1216C>G MANE Select	ENSP00000384957.2:p.His406Asp
ENST00000264692.8:c.1054C>G	ENSP00000264692.5:p.His352Asp
ENST00000403665.6:c.1216C>G	ENSP00000384957.2:p.His406Asp
NM_000128.3:c.1216C>G , LRG_583t1:c.1216C>G	NP_000119.1:p.His406Asp
XM_005262821.2:c.1219C>G	XP_005262878.1:p.His407Asp
XM_005262822.2:c.1219C>G	XP_005262879.1:p.His407Asp
XM_005262823.2:c.949C>G	XP_005262880.1:p.His317Asp
XM_005262824.1:c.1219C>G	XP_005262881.1:p.His407Asp
XM_006714137.1:c.1171C>G	XP_006714200.1:p.His391Asp
XR_938706.1:n.1624C>G
XR_938707.1:n.1624C>G
XM_005262821.4:c.1219C>G	XP_005262878.1:p.His407Asp
XM_005262822.4:c.1219C>G	XP_005262879.1:p.His407Asp
XM_005262823.4:c.949C>G	XP_005262880.1:p.His317Asp
XM_006714137.3:c.1171C>G	XP_006714200.1:p.His391Asp
XM_017007884.2:c.*2188C>G	XP_016863373.1:n.*2188C>G
XR_001741172.2:n.1690C>G
NM_000128.4:c.1216C>G MANE Select	NP_000119.1:p.His406Asp