Canonical Allele Identifier: CA388794221

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803679T>C (hg19) ; chr13:g.113149365T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149365T>C , CM000675.2:g.113149365T>C	GRCh38
NC_000013.10:g.113803679T>C , CM000675.1:g.113803679T>C	GRCh37
NC_000013.9:g.112851680T>C	NCBI36
NG_009258.1:g.31567T>C , LRG_548:g.31567T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1315T>C MANE Select	ENSP00000364709.3:p.Trp439Arg
ENST00000375551.7:c.*306T>C	ENSP00000364701.3:n.*306T>C
ENST00000375559.7:c.1315T>C	ENSP00000364709.3:p.Trp439Arg
ENST00000409306.5:c.*306T>C	ENSP00000387092.1:n.*306T>C
NM_000504.3:c.1315T>C , LRG_548t1:c.1315T>C	NP_000495.1:p.Trp439Arg
NM_001312674.1:c.1183T>C	NP_001299603.1:p.Trp395Arg
NM_001312675.1:c.*306T>C	NP_001299604.1:n.*306T>C
NM_000504.4:c.1315T>C MANE Select	NP_000495.1:p.Trp439Arg
NM_001312674.2:c.1183T>C	NP_001299603.1:p.Trp395Arg
NM_001312675.2:c.*306T>C	NP_001299604.1:n.*306T>C