Canonical Allele Identifier: CA3856113

Gene: EFHC1

Linked Data

• ClinVar Variation Id: 1140237
• ClinVar RCV Id: RCV003771474
• dbSNP Id: rs368238981
• ExAC: 6:52344472 C / T
• gnomAD v2: 6-52344472-C-T
• gnomAD v3: 6-52479674-C-T
• gnomAD v4: 6-52479674-C-T
• MyVariant Identifiers: chr6:g.52344472C>T (hg19) ; chr6:g.52479674C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479674C>T , CM000668.2:g.52479674C>T	GRCh38
NC_000006.11:g.52344472C>T , CM000668.1:g.52344472C>T	GRCh37
NC_000006.10:g.52452431C>T	NCBI36
NG_016760.1:g.64479C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1527C>T MANE Select	ENSP00000360107.4:p.Asp509=
ENST00000480623.6:c.1527C>T	ENSP00000434498.2:p.Asp509=
ENST00000635760.1:c.1203C>T	ENSP00000489765.1:p.Asp401=
ENST00000635812.1:c.*828C>T	ENSP00000490859.1:n.*828C>T
ENST00000635866.1:c.*1396C>T	ENSP00000489866.1:n.*1396C>T
ENST00000635911.1:n.3045C>T
ENST00000635984.1:c.1203C>T	ENSP00000489921.1:p.Asp401=
ENST00000635996.1:c.1527C>T	ENSP00000490256.1:p.Asp509=
ENST00000636107.1:c.1527C>T	ENSP00000489680.1:p.Asp509=
ENST00000636311.1:n.1421C>T
ENST00000636343.1:c.1193C>T
ENST00000636379.1:c.1239C>T	ENSP00000490622.1:p.Asp413=
ENST00000636398.1:c.1227C>T	ENSP00000489654.1:n.1227C>T
ENST00000636489.1:c.1470C>T	ENSP00000489998.1:p.Asp490=
ENST00000636616.1:n.1088C>T
ENST00000636702.1:c.1497C>T	ENSP00000489623.1:p.Asp499=
ENST00000636954.1:c.1470C>T	ENSP00000489966.1:p.Asp490=
ENST00000637089.1:c.1527C>T	ENSP00000489854.1:p.Asp509=
ENST00000637121.1:n.1329C>T
ENST00000637263.1:c.1527C>T	ENSP00000489700.1:p.Asp509=
ENST00000637340.1:n.3452C>T
ENST00000637353.1:c.1527C>T	ENSP00000490441.1:p.Asp509=
ENST00000637602.1:c.*1228C>T	ENSP00000490074.1:n.*1228C>T
ENST00000637849.1:n.1591C>T
ENST00000637874.1:c.472C>T	ENSP00000490348.1:n.472C>T
ENST00000637892.1:n.1731C>T
ENST00000371068.9:c.1527C>T	ENSP00000360107.4:p.Asp509=
ENST00000480623.5:c.*1947C>T	ENSP00000434498.1:n.*1947C>T
ENST00000538167.2:c.1470C>T	ENSP00000444521.1:p.Asp490=
NM_001172420.1:c.1470C>T	NP_001165891.1:p.Asp490=
NM_018100.3:c.1527C>T	NP_060570.2:p.Asp509=
NR_033327.1:n.2999C>T
NM_018100.4:c.1527C>T MANE Select	NP_060570.2:p.Asp509=
NM_001172420.2:c.1470C>T	NP_001165891.1:p.Asp490=
NR_033327.2:n.2853C>T