Canonical Allele Identifier: CA388793707
Gene: F10 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.113803577G>C (hg19) chr13:g.113149263G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149263G>C , CM000675.2:g.113149263G>C GRCh38
NC_000013.10:g.113803577G>C , CM000675.1:g.113803577G>C GRCh37
NC_000013.9:g.112851578G>C NCBI36
NG_009258.1:g.31465G>C , LRG_548:g.31465G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.1213G>C MANE Select ENSP00000364709.3:p.Ala405Pro
ENST00000375551.7:c.*204G>C ENSP00000364701.3:n.*204G>C
ENST00000375559.7:c.1213G>C ENSP00000364709.3:p.Ala405Pro
ENST00000409306.5:c.*204G>C ENSP00000387092.1:n.*204G>C
NM_000504.3:c.1213G>C , LRG_548t1:c.1213G>C NP_000495.1:p.Ala405Pro
NM_001312674.1:c.1081G>C NP_001299603.1:p.Ala361Pro
NM_001312675.1:c.*204G>C NP_001299604.1:n.*204G>C
NM_000504.4:c.1213G>C MANE Select NP_000495.1:p.Ala405Pro
NM_001312674.2:c.1081G>C NP_001299603.1:p.Ala361Pro
NM_001312675.2:c.*204G>C NP_001299604.1:n.*204G>C
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