Canonical Allele Identifier: CA364455660
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52465011T>A , CM000668.2:g.52465011T>A GRCh38
NC_000006.11:g.52329809T>A , CM000668.1:g.52329809T>A GRCh37
NC_000006.10:g.52437768T>A NCBI36
NG_016760.1:g.49816T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1033T>A MANE Select ENSP00000360107.4:p.Tyr345Asn
ENST00000480623.6:c.1033T>A ENSP00000434498.2:p.Tyr345Asn
ENST00000635760.1:c.709T>A ENSP00000489765.1:p.Tyr237Asn
ENST00000635812.1:c.*334T>A ENSP00000490859.1:n.*334T>A
ENST00000635866.1:c.*902T>A ENSP00000489866.1:n.*902T>A
ENST00000635911.1:n.2551T>A
ENST00000635984.1:c.709T>A ENSP00000489921.1:p.Tyr237Asn
ENST00000635996.1:c.1033T>A ENSP00000490256.1:p.Tyr345Asn
ENST00000636107.1:c.1033T>A ENSP00000489680.1:p.Tyr345Asn
ENST00000636311.1:n.927T>A
ENST00000636343.1:c.699T>A
ENST00000636379.1:c.745T>A ENSP00000490622.1:p.Tyr249Asn
ENST00000636398.1:c.733T>A ENSP00000489654.1:n.733T>A
ENST00000636489.1:c.976T>A ENSP00000489998.1:p.Tyr326Asn
ENST00000636616.1:n.649T>A
ENST00000636702.1:c.1003T>A ENSP00000489623.1:p.Tyr335Asn
ENST00000636954.1:c.976T>A ENSP00000489966.1:p.Tyr326Asn
ENST00000637089.1:c.1033T>A ENSP00000489854.1:p.Tyr345Asn
ENST00000637263.1:c.1033T>A ENSP00000489700.1:p.Tyr345Asn
ENST00000637340.1:n.2958T>A
ENST00000637353.1:c.1033T>A ENSP00000490441.1:p.Tyr345Asn
ENST00000637602.1:c.*734T>A ENSP00000490074.1:n.*734T>A
ENST00000637849.1:n.1097T>A
ENST00000637874.1:c.83-4322T>A ENSP00000490348.1:n.83-4322T>A
ENST00000637892.1:n.1237T>A
ENST00000371068.9:c.1033T>A ENSP00000360107.4:p.Tyr345Asn
ENST00000480623.5:c.*1453T>A ENSP00000434498.1:n.*1453T>A
ENST00000538167.2:c.976T>A ENSP00000444521.1:p.Tyr326Asn
NM_001172420.1:c.976T>A NP_001165891.1:p.Tyr326Asn
NM_018100.3:c.1033T>A NP_060570.2:p.Tyr345Asn
NR_033327.1:n.2505T>A
NM_018100.4:c.1033T>A MANE Select NP_060570.2:p.Tyr345Asn
NM_001172420.2:c.976T>A NP_001165891.1:p.Tyr326Asn
NR_033327.2:n.2359T>A