Canonical Allele Identifier: CA2120140842

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149465C= , CM000675.2:g.113149465C=	GRCh38
NC_000013.10:g.113803779C= , CM000675.1:g.113803779C=	GRCh37
NC_000013.9:g.112851780C=	NCBI36
NG_009258.1:g.31667C= , LRG_548:g.31667C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1415C= MANE Select	ENSP00000364709.3:p.Pro472=
ENST00000375551.7:c.*406C=	ENSP00000364701.3:n.*406C=
ENST00000375559.7:c.1415C=	ENSP00000364709.3:p.Pro472=
NM_000504.3:c.1415C= , LRG_548t1:c.1415C=	NP_000495.1:p.Pro472=
NM_001312674.1:c.1283C=	NP_001299603.1:p.Pro428=
NM_001312675.1:c.*406C=	NP_001299604.1:n.*406C=
NM_000504.4:c.1415C= MANE Select	NP_000495.1:p.Pro472=
NM_001312674.2:c.1283C=	NP_001299603.1:p.Pro428=
NM_001312675.2:c.*406C=	NP_001299604.1:n.*406C=