Canonical Allele Identifier: CA364457732
Gene: EFHC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.52479643T>C , CM000668.2:g.52479643T>C GRCh38
NC_000006.11:g.52344441T>C , CM000668.1:g.52344441T>C GRCh37
NC_000006.10:g.52452400T>C NCBI36
NG_016760.1:g.64448T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371068.11:c.1496T>C MANE Select ENSP00000360107.4:p.Phe499Ser
ENST00000480623.6:c.1496T>C ENSP00000434498.2:p.Phe499Ser
ENST00000635760.1:c.1172T>C ENSP00000489765.1:p.Phe391Ser
ENST00000635812.1:c.*797T>C ENSP00000490859.1:n.*797T>C
ENST00000635866.1:c.*1365T>C ENSP00000489866.1:n.*1365T>C
ENST00000635911.1:n.3014T>C
ENST00000635984.1:c.1172T>C ENSP00000489921.1:p.Phe391Ser
ENST00000635996.1:c.1496T>C ENSP00000490256.1:p.Phe499Ser
ENST00000636107.1:c.1496T>C ENSP00000489680.1:p.Phe499Ser
ENST00000636311.1:n.1390T>C
ENST00000636343.1:c.1162T>C
ENST00000636379.1:c.1208T>C ENSP00000490622.1:p.Phe403Ser
ENST00000636398.1:c.1196T>C ENSP00000489654.1:n.1196T>C
ENST00000636489.1:c.1439T>C ENSP00000489998.1:p.Phe480Ser
ENST00000636616.1:n.1057T>C
ENST00000636702.1:c.1466T>C ENSP00000489623.1:p.Phe489Ser
ENST00000636954.1:c.1439T>C ENSP00000489966.1:p.Phe480Ser
ENST00000637089.1:c.1496T>C ENSP00000489854.1:p.Phe499Ser
ENST00000637121.1:n.1298T>C
ENST00000637263.1:c.1496T>C ENSP00000489700.1:p.Phe499Ser
ENST00000637340.1:n.3421T>C
ENST00000637353.1:c.1496T>C ENSP00000490441.1:p.Phe499Ser
ENST00000637602.1:c.*1197T>C ENSP00000490074.1:n.*1197T>C
ENST00000637849.1:n.1560T>C
ENST00000637874.1:c.441T>C ENSP00000490348.1:n.441T>C
ENST00000637892.1:n.1700T>C
ENST00000371068.9:c.1496T>C ENSP00000360107.4:p.Phe499Ser
ENST00000480623.5:c.*1916T>C ENSP00000434498.1:n.*1916T>C
ENST00000538167.2:c.1439T>C ENSP00000444521.1:p.Phe480Ser
NM_001172420.1:c.1439T>C NP_001165891.1:p.Phe480Ser
NM_018100.3:c.1496T>C NP_060570.2:p.Phe499Ser
NR_033327.1:n.2968T>C
NM_018100.4:c.1496T>C MANE Select NP_060570.2:p.Phe499Ser
NM_001172420.2:c.1439T>C NP_001165891.1:p.Phe480Ser
NR_033327.2:n.2822T>C