Canonical Allele Identifier: CA388787398

Gene: F10 F10-AS1

Linked Data

• MyVariant Identifiers: chr13:g.113783768T>G (hg19) ; chr13:g.113129454T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113129454T>G , CM000675.2:g.113129454T>G	GRCh38
NC_000013.10:g.113783768T>G , CM000675.1:g.113783768T>G	GRCh37
NC_000013.9:g.112831769T>G	NCBI36
NG_009258.1:g.11656T>G , LRG_548:g.11656T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.73T>G (F10) MANE Select	ENSP00000364709.3:p.Phe25Val
ENST00000375551.7:c.73T>G (F10)	ENSP00000364701.3:p.Phe25Val
ENST00000375559.7:c.73T>G (F10)	ENSP00000364709.3:p.Phe25Val
ENST00000409306.5:c.73T>G (F10)	ENSP00000387092.1:p.Phe25Val
ENST00000410083.6:c.73T>G (F10)	ENSP00000386320.2:p.Phe25Val
ENST00000477269.5:n.110T>G (F10)
ENST00000483537.1:n.93T>G (F10)
NM_000504.3:c.73T>G , LRG_548t1:c.73T>G (F10)	NP_000495.1:p.Phe25Val
NM_001312674.1:c.73T>G (F10)	NP_001299603.1:p.Phe25Val
NM_001312675.1:c.73T>G (F10)	NP_001299604.1:p.Phe25Val
NR_126424.1:n.41+552A>C (F10-AS1)
NM_000504.4:c.73T>G (F10) MANE Select	NP_000495.1:p.Phe25Val
NM_001312674.2:c.73T>G (F10)	NP_001299603.1:p.Phe25Val
NM_001312675.2:c.73T>G (F10)	NP_001299604.1:p.Phe25Val