Canonical Allele Identifier: CA1628833309

Gene: EFHC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479733C= , CM000668.2:g.52479733C=	GRCh38
NC_000006.11:g.52344531C= , CM000668.1:g.52344531C=	GRCh37
NC_000006.10:g.52452490C=	NCBI36
NG_016760.1:g.64538C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1586C= MANE Select	ENSP00000360107.4:p.Ala529=
ENST00000480623.6:c.1586C=	ENSP00000434498.2:p.Ala529=
ENST00000635760.1:c.1262C=	ENSP00000489765.1:p.Ala421=
ENST00000635812.1:c.*887C=	ENSP00000490859.1:n.*887C=
ENST00000635866.1:c.*1455C=	ENSP00000489866.1:n.*1455C=
ENST00000635911.1:n.3104C=
ENST00000635984.1:c.1262C=	ENSP00000489921.1:p.Ala421=
ENST00000635996.1:c.1586C=	ENSP00000490256.1:p.Ala529=
ENST00000636107.1:c.1586C=	ENSP00000489680.1:p.Ala529=
ENST00000636311.1:n.1480C=
ENST00000636343.1:c.1252C=
ENST00000636379.1:c.1298C=	ENSP00000490622.1:p.Ala433=
ENST00000636398.1:c.1286C=	ENSP00000489654.1:n.1286C=
ENST00000636489.1:c.1529C=	ENSP00000489998.1:p.Ala510=
ENST00000636616.1:n.1147C=
ENST00000636702.1:c.1556C=	ENSP00000489623.1:p.Ala519=
ENST00000636954.1:c.1529C=	ENSP00000489966.1:p.Ala510=
ENST00000637089.1:c.1586C=	ENSP00000489854.1:p.Ala529=
ENST00000637121.1:n.1388C=
ENST00000637263.1:c.1586C=	ENSP00000489700.1:p.Ala529=
ENST00000637340.1:n.3511C=
ENST00000637353.1:c.1586C=	ENSP00000490441.1:p.Ala529=
ENST00000637602.1:c.*1287C=	ENSP00000490074.1:n.*1287C=
ENST00000637849.1:n.1650C=
ENST00000637892.1:n.1790C=
ENST00000371068.9:c.1586C=	ENSP00000360107.4:p.Ala529=
ENST00000480623.5:c.*2006C=	ENSP00000434498.1:n.*2006C=
ENST00000538167.2:c.1529C=	ENSP00000444521.1:p.Ala510=
NM_001172420.1:c.1529C=	NP_001165891.1:p.Ala510=
NM_018100.3:c.1586C=	NP_060570.2:p.Ala529=
NR_033327.1:n.3058C=
NM_018100.4:c.1586C= MANE Select	NP_060570.2:p.Ala529=
NM_001172420.2:c.1529C=	NP_001165891.1:p.Ala510=
NR_033327.2:n.2912C=