Canonical Allele Identifier: CA1628833167
Gene: EFHC1 HGNC NCBI

Linked Data

dbSNP Id: rs1765629071

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479685del , CM000668.2:g.52479685del GRCh38
NC_000006.11:g.52344483del , CM000668.1:g.52344483del GRCh37
NC_000006.10:g.52452442del NCBI36
NG_016760.1:g.64490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1538del MANE Select ENSP00000360107.4:p.Leu513Ter
ENST00000480623.6:c.1538del ENSP00000434498.2:p.Leu513Ter
ENST00000635760.1:c.1214del ENSP00000489765.1:p.Leu405Ter
ENST00000635812.1:c.*839del ENSP00000490859.1:n.*839del
ENST00000635866.1:c.*1407del ENSP00000489866.1:n.*1407del
ENST00000635911.1:n.3056del
ENST00000635984.1:c.1214del ENSP00000489921.1:p.Leu405Ter
ENST00000635996.1:c.1538del ENSP00000490256.1:p.Leu513Ter
ENST00000636107.1:c.1538del ENSP00000489680.1:p.Leu513Ter
ENST00000636311.1:n.1432del
ENST00000636343.1:c.1204del
ENST00000636379.1:c.1250del ENSP00000490622.1:p.Leu417Ter
ENST00000636398.1:c.1238del ENSP00000489654.1:n.1238del
ENST00000636489.1:c.1481del ENSP00000489998.1:p.Leu494Ter
ENST00000636616.1:n.1099del
ENST00000636702.1:c.1508del ENSP00000489623.1:p.Leu503Ter
ENST00000636954.1:c.1481del ENSP00000489966.1:p.Leu494Ter
ENST00000637089.1:c.1538del ENSP00000489854.1:p.Leu513Ter
ENST00000637121.1:n.1340del
ENST00000637263.1:c.1538del ENSP00000489700.1:p.Leu513Ter
ENST00000637340.1:n.3463del
ENST00000637353.1:c.1538del ENSP00000490441.1:p.Leu513Ter
ENST00000637602.1:c.*1239del ENSP00000490074.1:n.*1239del
ENST00000637849.1:n.1602del
ENST00000637874.1:c.483del ENSP00000490348.1:n.483del
ENST00000637892.1:n.1742del
ENST00000371068.9:c.1538del ENSP00000360107.4:p.Leu513Ter
ENST00000480623.5:c.*1958del ENSP00000434498.1:n.*1958del
ENST00000538167.2:c.1481del ENSP00000444521.1:p.Leu494Ter
NM_001172420.1:c.1481del NP_001165891.1:p.Leu494Ter
NM_018100.3:c.1538del NP_060570.2:p.Leu513Ter
NR_033327.1:n.3010del
NM_018100.4:c.1538del MANE Select NP_060570.2:p.Leu513Ter
NM_001172420.2:c.1481del NP_001165891.1:p.Leu494Ter
NR_033327.2:n.2864del