Canonical Allele Identifier: CA3856053

Gene: EFHC1

Linked Data

• dbSNP Id: rs777992546
• ExAC: 6:52343841 C / A
• gnomAD v2: 6-52343841-C-A
• gnomAD v4: 6-52479043-C-A
• MyVariant Identifiers: chr6:g.52343841C>A (hg19) ; chr6:g.52479043C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479043C>A , CM000668.2:g.52479043C>A	GRCh38
NC_000006.11:g.52343841C>A , CM000668.1:g.52343841C>A	GRCh37
NC_000006.10:g.52451800C>A	NCBI36
NG_016760.1:g.63848C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1285C>A MANE Select	ENSP00000360107.4:p.Pro429Thr
ENST00000480623.6:c.1285C>A	ENSP00000434498.2:p.Pro429Thr
ENST00000635760.1:c.961C>A	ENSP00000489765.1:p.Pro321Thr
ENST00000635812.1:c.*586C>A	ENSP00000490859.1:n.*586C>A
ENST00000635866.1:c.*1154C>A	ENSP00000489866.1:n.*1154C>A
ENST00000635911.1:n.2803C>A
ENST00000635984.1:c.961C>A	ENSP00000489921.1:p.Pro321Thr
ENST00000635996.1:c.1285C>A	ENSP00000490256.1:p.Pro429Thr
ENST00000636107.1:c.1285C>A	ENSP00000489680.1:p.Pro429Thr
ENST00000636311.1:n.1179C>A
ENST00000636343.1:c.951C>A
ENST00000636379.1:c.997C>A	ENSP00000490622.1:p.Pro333Thr
ENST00000636398.1:c.985C>A	ENSP00000489654.1:n.985C>A
ENST00000636489.1:c.1228C>A	ENSP00000489998.1:p.Pro410Thr
ENST00000636616.1:n.895-49C>A
ENST00000636702.1:c.1255C>A	ENSP00000489623.1:p.Pro419Thr
ENST00000636954.1:c.1228C>A	ENSP00000489966.1:p.Pro410Thr
ENST00000637089.1:c.1285C>A	ENSP00000489854.1:p.Pro429Thr
ENST00000637121.1:n.1087C>A
ENST00000637263.1:c.1285C>A	ENSP00000489700.1:p.Pro429Thr
ENST00000637340.1:n.3210C>A
ENST00000637353.1:c.1285C>A	ENSP00000490441.1:p.Pro429Thr
ENST00000637602.1:c.*986C>A	ENSP00000490074.1:n.*986C>A
ENST00000637849.1:n.1349C>A
ENST00000637874.1:c.230C>A	ENSP00000490348.1:n.230C>A
ENST00000637892.1:n.1489C>A
ENST00000371068.9:c.1285C>A	ENSP00000360107.4:p.Pro429Thr
ENST00000480623.5:c.*1705C>A	ENSP00000434498.1:n.*1705C>A
ENST00000538167.2:c.1228C>A	ENSP00000444521.1:p.Pro410Thr
NM_001172420.1:c.1228C>A	NP_001165891.1:p.Pro410Thr
NM_018100.3:c.1285C>A	NP_060570.2:p.Pro429Thr
NR_033327.1:n.2757C>A
NM_018100.4:c.1285C>A MANE Select	NP_060570.2:p.Pro429Thr
NM_001172420.2:c.1228C>A	NP_001165891.1:p.Pro410Thr
NR_033327.2:n.2611C>A