Canonical Allele Identifier: CA450423441

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52329718A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52464920A>G , CM000668.2:g.52464920A>G	GRCh38
NC_000006.11:g.52329718A>G , CM000668.1:g.52329718A>G	GRCh37
NC_000006.10:g.52437677A>G	NCBI36
NG_016760.1:g.49725A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.942A>G MANE Select	ENSP00000360107.4:p.Glu314=
ENST00000480623.6:c.942A>G	ENSP00000434498.2:p.Glu314=
ENST00000635760.1:c.618A>G	ENSP00000489765.1:p.Glu206=
ENST00000635812.1:c.*243A>G	ENSP00000490859.1:n.*243A>G
ENST00000635866.1:c.*811A>G	ENSP00000489866.1:n.*811A>G
ENST00000635911.1:n.2460A>G
ENST00000635984.1:c.618A>G	ENSP00000489921.1:p.Glu206=
ENST00000635996.1:c.942A>G	ENSP00000490256.1:p.Glu314=
ENST00000636107.1:c.942A>G	ENSP00000489680.1:p.Glu314=
ENST00000636311.1:n.836A>G
ENST00000636343.1:c.608A>G
ENST00000636379.1:c.654A>G	ENSP00000490622.1:p.Glu218=
ENST00000636398.1:c.642A>G	ENSP00000489654.1:n.642A>G
ENST00000636489.1:c.885A>G	ENSP00000489998.1:p.Glu295=
ENST00000636616.1:n.558A>G
ENST00000636702.1:c.912A>G	ENSP00000489623.1:p.Glu304=
ENST00000636954.1:c.885A>G	ENSP00000489966.1:p.Glu295=
ENST00000637089.1:c.942A>G	ENSP00000489854.1:p.Glu314=
ENST00000637263.1:c.942A>G	ENSP00000489700.1:p.Glu314=
ENST00000637340.1:n.2867A>G
ENST00000637353.1:c.942A>G	ENSP00000490441.1:p.Glu314=
ENST00000637602.1:c.*643A>G	ENSP00000490074.1:n.*643A>G
ENST00000637849.1:n.1006A>G
ENST00000637874.1:c.83-4413A>G	ENSP00000490348.1:n.83-4413A>G
ENST00000637892.1:n.1146A>G
ENST00000371068.9:c.942A>G	ENSP00000360107.4:p.Glu314=
ENST00000480623.5:c.*1362A>G	ENSP00000434498.1:n.*1362A>G
ENST00000538167.2:c.885A>G	ENSP00000444521.1:p.Glu295=
NM_001172420.1:c.885A>G	NP_001165891.1:p.Glu295=
NM_018100.3:c.942A>G	NP_060570.2:p.Glu314=
NR_033327.1:n.2414A>G
NM_018100.4:c.942A>G MANE Select	NP_060570.2:p.Glu314=
NM_001172420.2:c.885A>G	NP_001165891.1:p.Glu295=
NR_033327.2:n.2268A>G