Canonical Allele Identifier: CA485027341
Gene: F10 HGNC NCBI
F10-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.113783773C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113129459C>T , CM000675.2:g.113129459C>T GRCh38
NC_000013.10:g.113783773C>T , CM000675.1:g.113783773C>T GRCh37
NC_000013.9:g.112831774C>T NCBI36
NG_009258.1:g.11661C>T , LRG_548:g.11661C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375559.8:c.78C>T (F10) MANE Select ENSP00000364709.3:p.Ile26=
ENST00000375551.7:c.78C>T (F10) ENSP00000364701.3:p.Ile26=
ENST00000375559.7:c.78C>T (F10) ENSP00000364709.3:p.Ile26=
ENST00000409306.5:c.78C>T (F10) ENSP00000387092.1:p.Ile26=
ENST00000410083.6:c.78C>T (F10) ENSP00000386320.2:p.Ile26=
ENST00000477269.5:n.115C>T (F10)
ENST00000483537.1:n.98C>T (F10)
NM_000504.3:c.78C>T , LRG_548t1:c.78C>T (F10) NP_000495.1:p.Ile26=
NM_001312674.1:c.78C>T (F10) NP_001299603.1:p.Ile26=
NM_001312675.1:c.78C>T (F10) NP_001299604.1:p.Ile26=
NR_126424.1:n.41+547G>A (F10-AS1)
NM_000504.4:c.78C>T (F10) MANE Select NP_000495.1:p.Ile26=
NM_001312674.2:c.78C>T (F10) NP_001299603.1:p.Ile26=
NM_001312675.2:c.78C>T (F10) NP_001299604.1:p.Ile26=
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