Canonical Allele Identifier: CA358941891

Gene: F11

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1216C>T MANE Select	ENSP00000384957.2:p.His406Tyr
ENST00000264692.8:c.1054C>T	ENSP00000264692.5:p.His352Tyr
ENST00000403665.6:c.1216C>T	ENSP00000384957.2:p.His406Tyr
NM_000128.3:c.1216C>T , LRG_583t1:c.1216C>T	NP_000119.1:p.His406Tyr
XM_005262821.2:c.1219C>T	XP_005262878.1:p.His407Tyr
XM_005262822.2:c.1219C>T	XP_005262879.1:p.His407Tyr
XM_005262823.2:c.949C>T	XP_005262880.1:p.His317Tyr
XM_005262824.1:c.1219C>T	XP_005262881.1:p.His407Tyr
XM_006714137.1:c.1171C>T	XP_006714200.1:p.His391Tyr
XR_938706.1:n.1624C>T
XR_938707.1:n.1624C>T
XM_005262821.4:c.1219C>T	XP_005262878.1:p.His407Tyr
XM_005262822.4:c.1219C>T	XP_005262879.1:p.His407Tyr
XM_005262823.4:c.949C>T	XP_005262880.1:p.His317Tyr
XM_006714137.3:c.1171C>T	XP_006714200.1:p.His391Tyr
XM_017007884.2:c.*2188C>T	XP_016863373.1:n.*2188C>T
XR_001741172.2:n.1690C>T
NM_000128.4:c.1216C>T MANE Select	NP_000119.1:p.His406Tyr