Canonical Allele Identifier: CA388793771
Gene: F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.113803588C>A (hg19) chr13:g.113149274C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149274C>A , CM000675.2:g.113149274C>A GRCh38
NC_000013.10:g.113803588C>A , CM000675.1:g.113803588C>A GRCh37
NC_000013.9:g.112851589C>A NCBI36
NG_009258.1:g.31476C>A , LRG_548:g.31476C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1224C>A MANE Select ENSP00000364709.3:p.Asp408Glu
ENST00000375551.7:c.*215C>A ENSP00000364701.3:n.*215C>A
ENST00000375559.7:c.1224C>A ENSP00000364709.3:p.Asp408Glu
ENST00000409306.5:c.*215C>A ENSP00000387092.1:n.*215C>A
NM_000504.3:c.1224C>A , LRG_548t1:c.1224C>A NP_000495.1:p.Asp408Glu
NM_001312674.1:c.1092C>A NP_001299603.1:p.Asp364Glu
NM_001312675.1:c.*215C>A NP_001299604.1:n.*215C>A
NM_000504.4:c.1224C>A MANE Select NP_000495.1:p.Asp408Glu
NM_001312674.2:c.1092C>A NP_001299603.1:p.Asp364Glu
NM_001312675.2:c.*215C>A NP_001299604.1:n.*215C>A
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