Canonical Allele Identifier: CA358943151

Gene: F11

Linked Data

• dbSNP Id: rs1741152101
• MyVariant Identifiers: chr4:g.187206842C>T (hg19) ; chr4:g.186285688C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186285688C>T , CM000666.2:g.186285688C>T	GRCh38
NC_000004.11:g.187206842C>T , CM000666.1:g.187206842C>T	GRCh37
NC_000004.10:g.187443836C>T	NCBI36
NG_008051.1:g.24725C>T , LRG_583:g.24725C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.1355C>T MANE Select	ENSP00000384957.2:p.Ser452Phe
ENST00000264691.4:c.51C>T
ENST00000264692.8:c.1193C>T	ENSP00000264692.5:p.Ser398Phe
ENST00000403665.6:c.1355C>T	ENSP00000384957.2:p.Ser452Phe
NM_000128.3:c.1355C>T , LRG_583t1:c.1355C>T	NP_000119.1:p.Ser452Phe
XM_005262821.2:c.1358C>T	XP_005262878.1:p.Ser453Phe
XM_005262822.2:c.1358C>T	XP_005262879.1:p.Ser453Phe
XM_005262823.2:c.1088C>T	XP_005262880.1:p.Ser363Phe
XM_005262824.1:c.1358C>T	XP_005262881.1:p.Ser453Phe
XM_006714137.1:c.1310C>T	XP_006714200.1:p.Ser437Phe
XR_938706.1:n.1763C>T
XR_938707.1:n.1763C>T
XM_005262821.4:c.1358C>T	XP_005262878.1:p.Ser453Phe
XM_005262822.4:c.1358C>T	XP_005262879.1:p.Ser453Phe
XM_005262823.4:c.1088C>T	XP_005262880.1:p.Ser363Phe
XM_006714137.3:c.1310C>T	XP_006714200.1:p.Ser437Phe
XR_001741172.2:n.1829C>T
NM_000128.4:c.1355C>T MANE Select	NP_000119.1:p.Ser452Phe