Canonical Allele Identifier: CA485425331

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803780C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149466C>A , CM000675.2:g.113149466C>A	GRCh38
NC_000013.10:g.113803780C>A , CM000675.1:g.113803780C>A	GRCh37
NC_000013.9:g.112851781C>A	NCBI36
NG_009258.1:g.31668C>A , LRG_548:g.31668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1416C>A MANE Select	ENSP00000364709.3:p.Pro472=
ENST00000375551.7:c.*407C>A	ENSP00000364701.3:n.*407C>A
ENST00000375559.7:c.1416C>A	ENSP00000364709.3:p.Pro472=
NM_000504.3:c.1416C>A , LRG_548t1:c.1416C>A	NP_000495.1:p.Pro472=
NM_001312674.1:c.1284C>A	NP_001299603.1:p.Pro428=
NM_001312675.1:c.*407C>A	NP_001299604.1:n.*407C>A
NM_000504.4:c.1416C>A MANE Select	NP_000495.1:p.Pro472=
NM_001312674.2:c.1284C>A	NP_001299603.1:p.Pro428=
NM_001312675.2:c.*407C>A	NP_001299604.1:n.*407C>A