Canonical Allele Identifier: CA388787364

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113122916G>C , CM000675.2:g.113122916G>C	GRCh38
NC_000013.10:g.113777230G>C , CM000675.1:g.113777230G>C	GRCh37
NC_000013.9:g.112825231G>C	NCBI36
NG_009258.1:g.5118G>C , LRG_548:g.5118G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000504.4:c.61G>C MANE Select	NP_000495.1:p.Gly21Arg
ENST00000375559.8:c.61G>C MANE Select	ENSP00000364709.3:p.Gly21Arg
NM_000504.3:c.61G>C , LRG_548t1:c.61G>C	NP_000495.1:p.Gly21Arg
NM_001312674.1:c.61G>C	NP_001299603.1:p.Gly21Arg
NM_001312674.2:c.61G>C	NP_001299603.1:p.Gly21Arg
NM_001312675.1:c.61G>C	NP_001299604.1:p.Gly21Arg
NM_001312675.2:c.61G>C	NP_001299604.1:p.Gly21Arg
ENST00000375551.7:c.61G>C	ENSP00000364701.3:p.Gly21Arg
ENST00000375559.7:c.61G>C	ENSP00000364709.3:p.Gly21Arg
ENST00000409306.5:c.61G>C	ENSP00000387092.1:p.Gly21Arg
ENST00000410083.6:c.61G>C	ENSP00000386320.2:p.Gly21Arg
ENST00000477269.5:n.98G>C
ENST00000483537.1:n.81G>C