Canonical Allele Identifier: CA1628833319

Gene: EFHC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479738A= , CM000668.2:g.52479738A=	GRCh38
NC_000006.11:g.52344536A= , CM000668.1:g.52344536A=	GRCh37
NC_000006.10:g.52452495A=	NCBI36
NG_016760.1:g.64543A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1591A= MANE Select	ENSP00000360107.4:p.Ile531=
ENST00000480623.6:c.1591A=	ENSP00000434498.2:p.Ile531=
ENST00000635760.1:c.1267A=	ENSP00000489765.1:p.Ile423=
ENST00000635812.1:c.*892A=	ENSP00000490859.1:n.*892A=
ENST00000635866.1:c.*1460A=	ENSP00000489866.1:n.*1460A=
ENST00000635911.1:n.3109A=
ENST00000635984.1:c.1267A=	ENSP00000489921.1:p.Ile423=
ENST00000635996.1:c.1591A=	ENSP00000490256.1:p.Ile531=
ENST00000636107.1:c.1591A=	ENSP00000489680.1:p.Ile531=
ENST00000636311.1:n.1485A=
ENST00000636343.1:c.1257A=
ENST00000636379.1:c.1303A=	ENSP00000490622.1:p.Ile435=
ENST00000636398.1:c.1291A=	ENSP00000489654.1:n.1291A=
ENST00000636489.1:c.1534A=	ENSP00000489998.1:p.Ile512=
ENST00000636616.1:n.1152A=
ENST00000636702.1:c.1561A=	ENSP00000489623.1:p.Ile521=
ENST00000636954.1:c.1534A=	ENSP00000489966.1:p.Ile512=
ENST00000637089.1:c.1591A=	ENSP00000489854.1:p.Ile531=
ENST00000637121.1:n.1393A=
ENST00000637263.1:c.1591A=	ENSP00000489700.1:p.Ile531=
ENST00000637340.1:n.3516A=
ENST00000637353.1:c.1591A=	ENSP00000490441.1:p.Ile531=
ENST00000637602.1:c.*1292A=	ENSP00000490074.1:n.*1292A=
ENST00000637849.1:n.1655A=
ENST00000637892.1:n.1795A=
ENST00000371068.9:c.1591A=	ENSP00000360107.4:p.Ile531=
ENST00000480623.5:c.*2011A=	ENSP00000434498.1:n.*2011A=
ENST00000538167.2:c.1534A=	ENSP00000444521.1:p.Ile512=
NM_001172420.1:c.1534A=	NP_001165891.1:p.Ile512=
NM_018100.3:c.1591A=	NP_060570.2:p.Ile531=
NR_033327.1:n.3063A=
NM_018100.4:c.1591A= MANE Select	NP_060570.2:p.Ile531=
NM_001172420.2:c.1534A=	NP_001165891.1:p.Ile512=
NR_033327.2:n.2917A=