Canonical Allele Identifier: CA388793675

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803572T>G (hg19) ; chr13:g.113149258T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149258T>G , CM000675.2:g.113149258T>G	GRCh38
NC_000013.10:g.113803572T>G , CM000675.1:g.113803572T>G	GRCh37
NC_000013.9:g.112851573T>G	NCBI36
NG_009258.1:g.31460T>G , LRG_548:g.31460T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1208T>G MANE Select	ENSP00000364709.3:p.Phe403Cys
ENST00000375551.7:c.*199T>G	ENSP00000364701.3:n.*199T>G
ENST00000375559.7:c.1208T>G	ENSP00000364709.3:p.Phe403Cys
ENST00000409306.5:c.*199T>G	ENSP00000387092.1:n.*199T>G
NM_000504.3:c.1208T>G , LRG_548t1:c.1208T>G	NP_000495.1:p.Phe403Cys
NM_001312674.1:c.1076T>G	NP_001299603.1:p.Phe359Cys
NM_001312675.1:c.*199T>G	NP_001299604.1:n.*199T>G
NM_000504.4:c.1208T>G MANE Select	NP_000495.1:p.Phe403Cys
NM_001312674.2:c.1076T>G	NP_001299603.1:p.Phe359Cys
NM_001312675.2:c.*199T>G	NP_001299604.1:n.*199T>G