Canonical Allele Identifier: CA1628833293

Gene: EFHC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479728A= , CM000668.2:g.52479728A=	GRCh38
NC_000006.11:g.52344526A= , CM000668.1:g.52344526A=	GRCh37
NC_000006.10:g.52452485A=	NCBI36
NG_016760.1:g.64533A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1581A= MANE Select	ENSP00000360107.4:p.Ala527=
ENST00000480623.6:c.1581A=	ENSP00000434498.2:p.Ala527=
ENST00000635760.1:c.1257A=	ENSP00000489765.1:p.Ala419=
ENST00000635812.1:c.*882A=	ENSP00000490859.1:n.*882A=
ENST00000635866.1:c.*1450A=	ENSP00000489866.1:n.*1450A=
ENST00000635911.1:n.3099A=
ENST00000635984.1:c.1257A=	ENSP00000489921.1:p.Ala419=
ENST00000635996.1:c.1581A=	ENSP00000490256.1:p.Ala527=
ENST00000636107.1:c.1581A=	ENSP00000489680.1:p.Ala527=
ENST00000636311.1:n.1475A=
ENST00000636343.1:c.1247A=
ENST00000636379.1:c.1293A=	ENSP00000490622.1:p.Ala431=
ENST00000636398.1:c.1281A=	ENSP00000489654.1:n.1281A=
ENST00000636489.1:c.1524A=	ENSP00000489998.1:p.Ala508=
ENST00000636616.1:n.1142A=
ENST00000636702.1:c.1551A=	ENSP00000489623.1:p.Ala517=
ENST00000636954.1:c.1524A=	ENSP00000489966.1:p.Ala508=
ENST00000637089.1:c.1581A=	ENSP00000489854.1:p.Ala527=
ENST00000637121.1:n.1383A=
ENST00000637263.1:c.1581A=	ENSP00000489700.1:p.Ala527=
ENST00000637340.1:n.3506A=
ENST00000637353.1:c.1581A=	ENSP00000490441.1:p.Ala527=
ENST00000637602.1:c.*1282A=	ENSP00000490074.1:n.*1282A=
ENST00000637849.1:n.1645A=
ENST00000637892.1:n.1785A=
ENST00000371068.9:c.1581A=	ENSP00000360107.4:p.Ala527=
ENST00000480623.5:c.*2001A=	ENSP00000434498.1:n.*2001A=
ENST00000538167.2:c.1524A=	ENSP00000444521.1:p.Ala508=
NM_001172420.1:c.1524A=	NP_001165891.1:p.Ala508=
NM_018100.3:c.1581A=	NP_060570.2:p.Ala527=
NR_033327.1:n.3053A=
NM_018100.4:c.1581A= MANE Select	NP_060570.2:p.Ala527=
NM_001172420.2:c.1524A=	NP_001165891.1:p.Ala508=
NR_033327.2:n.2907A=