Canonical Allele Identifier: CA358941586

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187205266C>T (hg19) ; chr4:g.186284112C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186284112C>T , CM000666.2:g.186284112C>T	GRCh38
NC_000004.11:g.187205266C>T , CM000666.1:g.187205266C>T	GRCh37
NC_000004.10:g.187442260C>T	NCBI36
NG_008051.1:g.23149C>T , LRG_583:g.23149C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1156C>T MANE Select	ENSP00000384957.2:p.Pro386Ser
ENST00000264692.8:c.994C>T	ENSP00000264692.5:p.Pro332Ser
ENST00000403665.6:c.1156C>T	ENSP00000384957.2:p.Pro386Ser
NM_000128.3:c.1156C>T , LRG_583t1:c.1156C>T	NP_000119.1:p.Pro386Ser
XM_005262821.2:c.1159C>T	XP_005262878.1:p.Pro387Ser
XM_005262822.2:c.1159C>T	XP_005262879.1:p.Pro387Ser
XM_005262823.2:c.889C>T	XP_005262880.1:p.Pro297Ser
XM_005262824.1:c.1159C>T	XP_005262881.1:p.Pro387Ser
XM_006714137.1:c.1111C>T	XP_006714200.1:p.Pro371Ser
XR_938706.1:n.1564C>T
XR_938707.1:n.1564C>T
XM_005262821.4:c.1159C>T	XP_005262878.1:p.Pro387Ser
XM_005262822.4:c.1159C>T	XP_005262879.1:p.Pro387Ser
XM_005262823.4:c.889C>T	XP_005262880.1:p.Pro297Ser
XM_006714137.3:c.1111C>T	XP_006714200.1:p.Pro371Ser
XM_017007884.2:c.*2128C>T	XP_016863373.1:n.*2128C>T
XM_017007885.2:c.*24C>T	XP_016863374.1:n.*24C>T
XR_001741172.2:n.1630C>T
NM_000128.4:c.1156C>T MANE Select	NP_000119.1:p.Pro386Ser