Canonical Allele Identifier: CA1628820764
Gene: EFHC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52452755A= , CM000668.2:g.52452755A= GRCh38
NC_000006.11:g.52317553A= , CM000668.1:g.52317553A= GRCh37
NC_000006.10:g.52425512A= NCBI36
NG_016760.1:g.37560A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371068.11:c.641A= MANE Select ENSP00000360107.4:p.Glu214=
ENST00000480623.6:c.641A= ENSP00000434498.2:p.Glu214=
ENST00000635760.1:c.317A= ENSP00000489765.1:p.Glu106=
ENST00000635812.1:c.641A= ENSP00000490859.1:p.Glu214=
ENST00000635866.1:c.*510A= ENSP00000489866.1:n.*510A=
ENST00000635911.1:n.902A=
ENST00000635984.1:c.317A= ENSP00000489921.1:p.Glu106=
ENST00000635996.1:c.641A= ENSP00000490256.1:p.Glu214=
ENST00000636107.1:c.641A= ENSP00000489680.1:p.Glu214=
ENST00000636253.1:n.295A=
ENST00000636311.1:n.535A=
ENST00000636343.1:c.307A=
ENST00000636379.1:c.353A= ENSP00000490622.1:p.Glu118=
ENST00000636398.1:c.308A= ENSP00000489654.1:p.Glu103=
ENST00000636489.1:c.584A= ENSP00000489998.1:p.Glu195=
ENST00000636702.1:c.611A= ENSP00000489623.1:p.Glu204=
ENST00000636954.1:c.584A= ENSP00000489966.1:p.Glu195=
ENST00000637089.1:c.641A= ENSP00000489854.1:p.Glu214=
ENST00000637200.1:c.*657A= ENSP00000490567.1:n.*657A=
ENST00000637263.1:c.641A= ENSP00000489700.1:p.Glu214=
ENST00000637340.1:n.1309A=
ENST00000637353.1:c.641A= ENSP00000490441.1:p.Glu214=
ENST00000637602.1:c.*342A= ENSP00000490074.1:n.*342A=
ENST00000637849.1:n.705A=
ENST00000637892.1:n.845A=
ENST00000638075.1:c.23A= ENSP00000490711.1:p.Glu8=
ENST00000371068.9:c.641A= ENSP00000360107.4:p.Glu214=
ENST00000480623.5:c.641A= ENSP00000434498.1:p.Glu214=
ENST00000538167.2:c.584A= ENSP00000444521.1:p.Glu195=
NM_001172420.1:c.584A= NP_001165891.1:p.Glu195=
NM_018100.3:c.641A= NP_060570.2:p.Glu214=
NR_033327.1:n.856A=
NM_018100.4:c.641A= MANE Select NP_060570.2:p.Glu214=
NM_001172420.2:c.584A= NP_001165891.1:p.Glu195=
NR_033327.2:n.710A=