Canonical Allele Identifier: CA450427439

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52344463T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479665T>A , CM000668.2:g.52479665T>A	GRCh38
NC_000006.11:g.52344463T>A , CM000668.1:g.52344463T>A	GRCh37
NC_000006.10:g.52452422T>A	NCBI36
NG_016760.1:g.64470T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371068.11:c.1518T>A MANE Select	ENSP00000360107.4:p.Leu506=
ENST00000480623.6:c.1518T>A	ENSP00000434498.2:p.Leu506=
ENST00000635760.1:c.1194T>A	ENSP00000489765.1:p.Leu398=
ENST00000635812.1:c.*819T>A	ENSP00000490859.1:n.*819T>A
ENST00000635866.1:c.*1387T>A	ENSP00000489866.1:n.*1387T>A
ENST00000635911.1:n.3036T>A
ENST00000635984.1:c.1194T>A	ENSP00000489921.1:p.Leu398=
ENST00000635996.1:c.1518T>A	ENSP00000490256.1:p.Leu506=
ENST00000636107.1:c.1518T>A	ENSP00000489680.1:p.Leu506=
ENST00000636311.1:n.1412T>A
ENST00000636343.1:c.1184T>A
ENST00000636379.1:c.1230T>A	ENSP00000490622.1:p.Leu410=
ENST00000636398.1:c.1218T>A	ENSP00000489654.1:n.1218T>A
ENST00000636489.1:c.1461T>A	ENSP00000489998.1:p.Leu487=
ENST00000636616.1:n.1079T>A
ENST00000636702.1:c.1488T>A	ENSP00000489623.1:p.Leu496=
ENST00000636954.1:c.1461T>A	ENSP00000489966.1:p.Leu487=
ENST00000637089.1:c.1518T>A	ENSP00000489854.1:p.Leu506=
ENST00000637121.1:n.1320T>A
ENST00000637263.1:c.1518T>A	ENSP00000489700.1:p.Leu506=
ENST00000637340.1:n.3443T>A
ENST00000637353.1:c.1518T>A	ENSP00000490441.1:p.Leu506=
ENST00000637602.1:c.*1219T>A	ENSP00000490074.1:n.*1219T>A
ENST00000637849.1:n.1582T>A
ENST00000637874.1:c.463T>A	ENSP00000490348.1:n.463T>A
ENST00000637892.1:n.1722T>A
ENST00000371068.9:c.1518T>A	ENSP00000360107.4:p.Leu506=
ENST00000480623.5:c.*1938T>A	ENSP00000434498.1:n.*1938T>A
ENST00000538167.2:c.1461T>A	ENSP00000444521.1:p.Leu487=
NM_001172420.1:c.1461T>A	NP_001165891.1:p.Leu487=
NM_018100.3:c.1518T>A	NP_060570.2:p.Leu506=
NR_033327.1:n.2990T>A
NM_018100.4:c.1518T>A MANE Select	NP_060570.2:p.Leu506=
NM_001172420.2:c.1461T>A	NP_001165891.1:p.Leu487=
NR_033327.2:n.2844T>A