Canonical Allele Identifier: CA388792572

Gene: F10

Linked Data

• MyVariant Identifiers: chr13:g.113803373A>G (hg19) ; chr13:g.113149059A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149059A>G , CM000675.2:g.113149059A>G	GRCh38
NC_000013.10:g.113803373A>G , CM000675.1:g.113803373A>G	GRCh37
NC_000013.9:g.112851374A>G	NCBI36
NG_009258.1:g.31261A>G , LRG_548:g.31261A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1009A>G MANE Select	ENSP00000364709.3:p.Asn337Asp
ENST00000375551.7:c.999A>G	ENSP00000364701.3:p.Ter333Trp
ENST00000375559.7:c.1009A>G	ENSP00000364709.3:p.Asn337Asp
ENST00000409306.5:c.1005A>G	ENSP00000387092.1:p.Ter335Trp
NM_000504.3:c.1009A>G , LRG_548t1:c.1009A>G	NP_000495.1:p.Asn337Asp
NM_001312674.1:c.877A>G	NP_001299603.1:p.Asn293Asp
NM_001312675.1:c.999A>G	NP_001299604.1:p.Ter333Trp
NM_000504.4:c.1009A>G MANE Select	NP_000495.1:p.Asn337Asp
NM_001312674.2:c.877A>G	NP_001299603.1:p.Asn293Asp
NM_001312675.2:c.999A>G	NP_001299604.1:p.Ter333Trp