Canonical Allele Identifier: CA2120143047

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118965C= , CM000675.2:g.113118965C=	GRCh38
NC_000013.10:g.113773279C= , CM000675.1:g.113773279C=	GRCh37
NC_000013.9:g.112821280C=	NCBI36
NG_009258.1:g.1167C= , LRG_548:g.1167C=
NG_009262.1:g.18175C= , LRG_554:g.18175C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1292C= MANE Select	ENSP00000329546.4:p.Ser431=
ENST00000346342.7:c.1292C=	ENSP00000329546.3:p.Ser431=
ENST00000375581.3:c.1358C=	ENSP00000364731.3:p.Ser453=
ENST00000541084.5:c.1106C=	ENSP00000442051.2:p.Ser369=
NM_000131.4:c.1358C= , LRG_554t1:c.1358C=	NP_000122.1:p.Ser453=
NM_001267554.1:c.1106C=	NP_001254483.1:p.Ser369=
NM_019616.3:c.1292C= , LRG_554t2:c.1292C=	NP_062562.1:p.Ser431=
NR_051961.1:n.1379C=
XM_006719963.2:c.1151C=	XP_006720026.1:p.Ser384=
XM_011537474.1:c.1400C=	XP_011535776.1:p.Ser467=
XM_011537475.1:c.1214C=	XP_011535777.1:p.Ser405=
XM_011537476.1:c.1052C=	XP_011535778.1:p.Ser351=
XM_011537477.1:c.1361C=	XP_011535779.1:p.Ser454=
XM_006719963.3:c.1196C=	XP_006720026.2:p.Ser399=
XM_011537474.2:c.1445C=	XP_011535776.2:p.Ser482=
XM_011537475.2:c.1259C=	XP_011535777.2:p.Ser420=
XM_011537476.2:c.1052C=	XP_011535778.1:p.Ser351=
NM_019616.4:c.1292C= MANE Select	NP_062562.1:p.Ser431=
NR_051961.2:n.1376C=
NM_001267554.2:c.1106C=	NP_001254483.1:p.Ser369=