Canonical Allele Identifier: CA450427442

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52344466T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479668T>C , CM000668.2:g.52479668T>C	GRCh38
NC_000006.11:g.52344466T>C , CM000668.1:g.52344466T>C	GRCh37
NC_000006.10:g.52452425T>C	NCBI36
NG_016760.1:g.64473T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371068.11:c.1521T>C MANE Select	ENSP00000360107.4:p.Asp507=
ENST00000480623.6:c.1521T>C	ENSP00000434498.2:p.Asp507=
ENST00000635760.1:c.1197T>C	ENSP00000489765.1:p.Asp399=
ENST00000635812.1:c.*822T>C	ENSP00000490859.1:n.*822T>C
ENST00000635866.1:c.*1390T>C	ENSP00000489866.1:n.*1390T>C
ENST00000635911.1:n.3039T>C
ENST00000635984.1:c.1197T>C	ENSP00000489921.1:p.Asp399=
ENST00000635996.1:c.1521T>C	ENSP00000490256.1:p.Asp507=
ENST00000636107.1:c.1521T>C	ENSP00000489680.1:p.Asp507=
ENST00000636311.1:n.1415T>C
ENST00000636343.1:c.1187T>C
ENST00000636379.1:c.1233T>C	ENSP00000490622.1:p.Asp411=
ENST00000636398.1:c.1221T>C	ENSP00000489654.1:n.1221T>C
ENST00000636489.1:c.1464T>C	ENSP00000489998.1:p.Asp488=
ENST00000636616.1:n.1082T>C
ENST00000636702.1:c.1491T>C	ENSP00000489623.1:p.Asp497=
ENST00000636954.1:c.1464T>C	ENSP00000489966.1:p.Asp488=
ENST00000637089.1:c.1521T>C	ENSP00000489854.1:p.Asp507=
ENST00000637121.1:n.1323T>C
ENST00000637263.1:c.1521T>C	ENSP00000489700.1:p.Asp507=
ENST00000637340.1:n.3446T>C
ENST00000637353.1:c.1521T>C	ENSP00000490441.1:p.Asp507=
ENST00000637602.1:c.*1222T>C	ENSP00000490074.1:n.*1222T>C
ENST00000637849.1:n.1585T>C
ENST00000637874.1:c.466T>C	ENSP00000490348.1:n.466T>C
ENST00000637892.1:n.1725T>C
ENST00000371068.9:c.1521T>C	ENSP00000360107.4:p.Asp507=
ENST00000480623.5:c.*1941T>C	ENSP00000434498.1:n.*1941T>C
ENST00000538167.2:c.1464T>C	ENSP00000444521.1:p.Asp488=
NM_001172420.1:c.1464T>C	NP_001165891.1:p.Asp488=
NM_018100.3:c.1521T>C	NP_060570.2:p.Asp507=
NR_033327.1:n.2993T>C
NM_018100.4:c.1521T>C MANE Select	NP_060570.2:p.Asp507=
NM_001172420.2:c.1464T>C	NP_001165891.1:p.Asp488=
NR_033327.2:n.2847T>C