Canonical Allele Identifier: CA485027415

Gene: F10 F10-AS1

Linked Data

• gnomAD v4: 13-113129495-C-T
• MyVariant Identifiers: chr13:g.113783809C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113129495C>T , CM000675.2:g.113129495C>T	GRCh38
NC_000013.10:g.113783809C>T , CM000675.1:g.113783809C>T	GRCh37
NC_000013.9:g.112831810C>T	NCBI36
NG_009258.1:g.11697C>T , LRG_548:g.11697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.114C>T (F10) MANE Select	ENSP00000364709.3:p.Val38=
ENST00000375551.7:c.114C>T (F10)	ENSP00000364701.3:p.Val38=
ENST00000375559.7:c.114C>T (F10)	ENSP00000364709.3:p.Val38=
ENST00000409306.5:c.114C>T (F10)	ENSP00000387092.1:p.Val38=
ENST00000410083.6:c.114C>T (F10)	ENSP00000386320.2:p.Val38=
ENST00000477269.5:n.151C>T (F10)
ENST00000483537.1:n.134C>T (F10)
NM_000504.3:c.114C>T , LRG_548t1:c.114C>T (F10)	NP_000495.1:p.Val38=
NM_001312674.1:c.114C>T (F10)	NP_001299603.1:p.Val38=
NM_001312675.1:c.114C>T (F10)	NP_001299604.1:p.Val38=
NR_126424.1:n.41+511G>A (F10-AS1)
NM_000504.4:c.114C>T (F10) MANE Select	NP_000495.1:p.Val38=
NM_001312674.2:c.114C>T (F10)	NP_001299603.1:p.Val38=
NM_001312675.2:c.114C>T (F10)	NP_001299604.1:p.Val38=