Canonical Allele Identifier: CA364457782

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52344449C>G (hg19) ; chr6:g.52479651C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479651C>G , CM000668.2:g.52479651C>G	GRCh38
NC_000006.11:g.52344449C>G , CM000668.1:g.52344449C>G	GRCh37
NC_000006.10:g.52452408C>G	NCBI36
NG_016760.1:g.64456C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1504C>G MANE Select	ENSP00000360107.4:p.Arg502Gly
ENST00000480623.6:c.1504C>G	ENSP00000434498.2:p.Arg502Gly
ENST00000635760.1:c.1180C>G	ENSP00000489765.1:p.Arg394Gly
ENST00000635812.1:c.*805C>G	ENSP00000490859.1:n.*805C>G
ENST00000635866.1:c.*1373C>G	ENSP00000489866.1:n.*1373C>G
ENST00000635911.1:n.3022C>G
ENST00000635984.1:c.1180C>G	ENSP00000489921.1:p.Arg394Gly
ENST00000635996.1:c.1504C>G	ENSP00000490256.1:p.Arg502Gly
ENST00000636107.1:c.1504C>G	ENSP00000489680.1:p.Arg502Gly
ENST00000636311.1:n.1398C>G
ENST00000636343.1:c.1170C>G
ENST00000636379.1:c.1216C>G	ENSP00000490622.1:p.Arg406Gly
ENST00000636398.1:c.1204C>G	ENSP00000489654.1:n.1204C>G
ENST00000636489.1:c.1447C>G	ENSP00000489998.1:p.Arg483Gly
ENST00000636616.1:n.1065C>G
ENST00000636702.1:c.1474C>G	ENSP00000489623.1:p.Arg492Gly
ENST00000636954.1:c.1447C>G	ENSP00000489966.1:p.Arg483Gly
ENST00000637089.1:c.1504C>G	ENSP00000489854.1:p.Arg502Gly
ENST00000637121.1:n.1306C>G
ENST00000637263.1:c.1504C>G	ENSP00000489700.1:p.Arg502Gly
ENST00000637340.1:n.3429C>G
ENST00000637353.1:c.1504C>G	ENSP00000490441.1:p.Arg502Gly
ENST00000637602.1:c.*1205C>G	ENSP00000490074.1:n.*1205C>G
ENST00000637849.1:n.1568C>G
ENST00000637874.1:c.449C>G	ENSP00000490348.1:n.449C>G
ENST00000637892.1:n.1708C>G
ENST00000371068.9:c.1504C>G	ENSP00000360107.4:p.Arg502Gly
ENST00000480623.5:c.*1924C>G	ENSP00000434498.1:n.*1924C>G
ENST00000538167.2:c.1447C>G	ENSP00000444521.1:p.Arg483Gly
NM_001172420.1:c.1447C>G	NP_001165891.1:p.Arg483Gly
NM_018100.3:c.1504C>G	NP_060570.2:p.Arg502Gly
NR_033327.1:n.2976C>G
NM_018100.4:c.1504C>G MANE Select	NP_060570.2:p.Arg502Gly
NM_001172420.2:c.1447C>G	NP_001165891.1:p.Arg483Gly
NR_033327.2:n.2830C>G