Canonical Allele Identifier: CA364455607

Gene: EFHC1

Linked Data

• gnomAD v4: 6-52464985-C-G
• MyVariant Identifiers: chr6:g.52329783C>G (hg19) ; chr6:g.52464985C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52464985C>G , CM000668.2:g.52464985C>G	GRCh38
NC_000006.11:g.52329783C>G , CM000668.1:g.52329783C>G	GRCh37
NC_000006.10:g.52437742C>G	NCBI36
NG_016760.1:g.49790C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1007C>G MANE Select	ENSP00000360107.4:p.Thr336Ser
ENST00000480623.6:c.1007C>G	ENSP00000434498.2:p.Thr336Ser
ENST00000635760.1:c.683C>G	ENSP00000489765.1:p.Thr228Ser
ENST00000635812.1:c.*308C>G	ENSP00000490859.1:n.*308C>G
ENST00000635866.1:c.*876C>G	ENSP00000489866.1:n.*876C>G
ENST00000635911.1:n.2525C>G
ENST00000635984.1:c.683C>G	ENSP00000489921.1:p.Thr228Ser
ENST00000635996.1:c.1007C>G	ENSP00000490256.1:p.Thr336Ser
ENST00000636107.1:c.1007C>G	ENSP00000489680.1:p.Thr336Ser
ENST00000636311.1:n.901C>G
ENST00000636343.1:c.673C>G
ENST00000636379.1:c.719C>G	ENSP00000490622.1:p.Thr240Ser
ENST00000636398.1:c.707C>G	ENSP00000489654.1:n.707C>G
ENST00000636489.1:c.950C>G	ENSP00000489998.1:p.Thr317Ser
ENST00000636616.1:n.623C>G
ENST00000636702.1:c.977C>G	ENSP00000489623.1:p.Thr326Ser
ENST00000636954.1:c.950C>G	ENSP00000489966.1:p.Thr317Ser
ENST00000637089.1:c.1007C>G	ENSP00000489854.1:p.Thr336Ser
ENST00000637263.1:c.1007C>G	ENSP00000489700.1:p.Thr336Ser
ENST00000637340.1:n.2932C>G
ENST00000637353.1:c.1007C>G	ENSP00000490441.1:p.Thr336Ser
ENST00000637602.1:c.*708C>G	ENSP00000490074.1:n.*708C>G
ENST00000637849.1:n.1071C>G
ENST00000637874.1:c.83-4348C>G	ENSP00000490348.1:n.83-4348C>G
ENST00000637892.1:n.1211C>G
ENST00000371068.9:c.1007C>G	ENSP00000360107.4:p.Thr336Ser
ENST00000480623.5:c.*1427C>G	ENSP00000434498.1:n.*1427C>G
ENST00000538167.2:c.950C>G	ENSP00000444521.1:p.Thr317Ser
NM_001172420.1:c.950C>G	NP_001165891.1:p.Thr317Ser
NM_018100.3:c.1007C>G	NP_060570.2:p.Thr336Ser
NR_033327.1:n.2479C>G
NM_018100.4:c.1007C>G MANE Select	NP_060570.2:p.Thr336Ser
NM_001172420.2:c.950C>G	NP_001165891.1:p.Thr317Ser
NR_033327.2:n.2333C>G