Canonical Allele Identifier: CA2120128100

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113139537A= , CM000675.2:g.113139537A=	GRCh38
NC_000013.10:g.113793851A= , CM000675.1:g.113793851A=	GRCh37
NC_000013.9:g.112841852A=	NCBI36
NG_009258.1:g.21739A= , LRG_548:g.21739A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.370+67A= MANE Select	ENSP00000364709.3:n.370+67A=
ENST00000375551.7:c.370+67A=	ENSP00000364701.3:n.370+67A=
ENST00000375559.7:c.370+67A=	ENSP00000364709.3:n.370+67A=
ENST00000409306.5:c.370+67A=	ENSP00000387092.1:n.370+67A=
ENST00000410083.6:c.370+67A=	ENSP00000386320.2:n.370+67A=
ENST00000477269.5:n.407+67A=
NM_000504.3:c.370+67A= , LRG_548t1:c.370+67A=	NP_000495.1:n.370+67A=
NM_001312674.1:c.370+67A=	NP_001299603.1:n.370+67A=
NM_001312675.1:c.370+67A=	NP_001299604.1:n.370+67A=
NM_000504.4:c.370+67A= MANE Select	NP_000495.1:n.370+67A=
NM_001312674.2:c.370+67A=	NP_001299603.1:n.370+67A=
NM_001312675.2:c.370+67A=	NP_001299604.1:n.370+67A=