Canonical Allele Identifier: CA388793861
Gene: F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.113803602A>C (hg19) chr13:g.113149288A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149288A>C , CM000675.2:g.113149288A>C GRCh38
NC_000013.10:g.113803602A>C , CM000675.1:g.113803602A>C GRCh37
NC_000013.9:g.112851603A>C NCBI36
NG_009258.1:g.31490A>C , LRG_548:g.31490A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1238A>C MANE Select ENSP00000364709.3:p.Asp413Ala
ENST00000375551.7:c.*229A>C ENSP00000364701.3:n.*229A>C
ENST00000375559.7:c.1238A>C ENSP00000364709.3:p.Asp413Ala
ENST00000409306.5:c.*229A>C ENSP00000387092.1:n.*229A>C
NM_000504.3:c.1238A>C , LRG_548t1:c.1238A>C NP_000495.1:p.Asp413Ala
NM_001312674.1:c.1106A>C NP_001299603.1:p.Asp369Ala
NM_001312675.1:c.*229A>C NP_001299604.1:n.*229A>C
NM_000504.4:c.1238A>C MANE Select NP_000495.1:p.Asp413Ala
NM_001312674.2:c.1106A>C NP_001299603.1:p.Asp369Ala
NM_001312675.2:c.*229A>C NP_001299604.1:n.*229A>C
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