Canonical Allele Identifier: CA1628820758

Gene: EFHC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52452742G= , CM000668.2:g.52452742G=	GRCh38
NC_000006.11:g.52317540G= , CM000668.1:g.52317540G=	GRCh37
NC_000006.10:g.52425499G=	NCBI36
NG_016760.1:g.37547G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371068.11:c.628G= MANE Select	ENSP00000360107.4:p.Asp210=
ENST00000480623.6:c.628G=	ENSP00000434498.2:p.Asp210=
ENST00000635760.1:c.304G=	ENSP00000489765.1:p.Asp102=
ENST00000635812.1:c.628G=	ENSP00000490859.1:p.Asp210=
ENST00000635866.1:c.*497G=	ENSP00000489866.1:n.*497G=
ENST00000635911.1:n.889G=
ENST00000635984.1:c.304G=	ENSP00000489921.1:p.Asp102=
ENST00000635996.1:c.628G=	ENSP00000490256.1:p.Asp210=
ENST00000636107.1:c.628G=	ENSP00000489680.1:p.Asp210=
ENST00000636253.1:n.282G=
ENST00000636311.1:n.522G=
ENST00000636343.1:c.294G=
ENST00000636379.1:c.340G=	ENSP00000490622.1:p.Asp114=
ENST00000636398.1:c.295G=	ENSP00000489654.1:p.Asp99=
ENST00000636489.1:c.571G=	ENSP00000489998.1:p.Asp191=
ENST00000636702.1:c.598G=	ENSP00000489623.1:p.Asp200=
ENST00000636954.1:c.571G=	ENSP00000489966.1:p.Asp191=
ENST00000637089.1:c.628G=	ENSP00000489854.1:p.Asp210=
ENST00000637200.1:c.*644G=	ENSP00000490567.1:n.*644G=
ENST00000637263.1:c.628G=	ENSP00000489700.1:p.Asp210=
ENST00000637340.1:n.1296G=
ENST00000637353.1:c.628G=	ENSP00000490441.1:p.Asp210=
ENST00000637602.1:c.*329G=	ENSP00000490074.1:n.*329G=
ENST00000637849.1:n.692G=
ENST00000637892.1:n.832G=
ENST00000638075.1:c.10G=	ENSP00000490711.1:p.Asp4=
ENST00000371068.9:c.628G=	ENSP00000360107.4:p.Asp210=
ENST00000480623.5:c.628G=	ENSP00000434498.1:p.Asp210=
ENST00000538167.2:c.571G=	ENSP00000444521.1:p.Asp191=
NM_001172420.1:c.571G=	NP_001165891.1:p.Asp191=
NM_018100.3:c.628G=	NP_060570.2:p.Asp210=
NR_033327.1:n.843G=
NM_018100.4:c.628G= MANE Select	NP_060570.2:p.Asp210=
NM_001172420.2:c.571G=	NP_001165891.1:p.Asp191=
NR_033327.2:n.697G=