Canonical Allele Identifier: CA2018046983

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149337C= , CM000675.2:g.113149337C=	GRCh38
NC_000013.10:g.113803651C= , CM000675.1:g.113803651C=	GRCh37
NC_000013.9:g.112851652C=	NCBI36
NG_009258.1:g.31539C= , LRG_548:g.31539C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1287C= MANE Select	ENSP00000364709.3:p.Asp429=
ENST00000375551.7:c.*278C=	ENSP00000364701.3:n.*278C=
ENST00000375559.7:c.1287C=	ENSP00000364709.3:p.Asp429=
ENST00000409306.5:c.*278C=	ENSP00000387092.1:n.*278C=
NM_000504.3:c.1287C= , LRG_548t1:c.1287C=	NP_000495.1:p.Asp429=
NM_001312674.1:c.1155C=	NP_001299603.1:p.Asp385=
NM_001312675.1:c.*278C=	NP_001299604.1:n.*278C=
NM_000504.4:c.1287C= MANE Select	NP_000495.1:p.Asp429=
NM_001312674.2:c.1155C=	NP_001299603.1:p.Asp385=
NM_001312675.2:c.*278C=	NP_001299604.1:n.*278C=