Canonical Allele Identifier: CA450427317

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52343894C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479096C>A , CM000668.2:g.52479096C>A	GRCh38
NC_000006.11:g.52343894C>A , CM000668.1:g.52343894C>A	GRCh37
NC_000006.10:g.52451853C>A	NCBI36
NG_016760.1:g.63901C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1338C>A MANE Select	ENSP00000360107.4:p.Thr446=
ENST00000480623.6:c.1338C>A	ENSP00000434498.2:p.Thr446=
ENST00000635760.1:c.1014C>A	ENSP00000489765.1:p.Thr338=
ENST00000635812.1:c.*639C>A	ENSP00000490859.1:n.*639C>A
ENST00000635866.1:c.*1207C>A	ENSP00000489866.1:n.*1207C>A
ENST00000635911.1:n.2856C>A
ENST00000635984.1:c.1014C>A	ENSP00000489921.1:p.Thr338=
ENST00000635996.1:c.1338C>A	ENSP00000490256.1:p.Thr446=
ENST00000636107.1:c.1338C>A	ENSP00000489680.1:p.Thr446=
ENST00000636311.1:n.1232C>A
ENST00000636343.1:c.1004C>A
ENST00000636379.1:c.1050C>A	ENSP00000490622.1:p.Thr350=
ENST00000636398.1:c.1038C>A	ENSP00000489654.1:n.1038C>A
ENST00000636489.1:c.1281C>A	ENSP00000489998.1:p.Thr427=
ENST00000636616.1:n.899C>A
ENST00000636702.1:c.1308C>A	ENSP00000489623.1:p.Thr436=
ENST00000636954.1:c.1281C>A	ENSP00000489966.1:p.Thr427=
ENST00000637089.1:c.1338C>A	ENSP00000489854.1:p.Thr446=
ENST00000637121.1:n.1140C>A
ENST00000637263.1:c.1338C>A	ENSP00000489700.1:p.Thr446=
ENST00000637340.1:n.3263C>A
ENST00000637353.1:c.1338C>A	ENSP00000490441.1:p.Thr446=
ENST00000637602.1:c.*1039C>A	ENSP00000490074.1:n.*1039C>A
ENST00000637849.1:n.1402C>A
ENST00000637874.1:c.283C>A	ENSP00000490348.1:n.283C>A
ENST00000637892.1:n.1542C>A
ENST00000371068.9:c.1338C>A	ENSP00000360107.4:p.Thr446=
ENST00000480623.5:c.*1758C>A	ENSP00000434498.1:n.*1758C>A
ENST00000538167.2:c.1281C>A	ENSP00000444521.1:p.Thr427=
NM_001172420.1:c.1281C>A	NP_001165891.1:p.Thr427=
NM_018100.3:c.1338C>A	NP_060570.2:p.Thr446=
NR_033327.1:n.2810C>A
NM_018100.4:c.1338C>A MANE Select	NP_060570.2:p.Thr446=
NM_001172420.2:c.1281C>A	NP_001165891.1:p.Thr427=
NR_033327.2:n.2664C>A