Canonical Allele Identifier: CA364452078

Gene: EFHC1

Linked Data

• gnomAD v4: 6-52452745-C-A
• MyVariant Identifiers: chr6:g.52317543C>A (hg19) ; chr6:g.52452745C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52452745C>A , CM000668.2:g.52452745C>A	GRCh38
NC_000006.11:g.52317543C>A , CM000668.1:g.52317543C>A	GRCh37
NC_000006.10:g.52425502C>A	NCBI36
NG_016760.1:g.37550C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371068.11:c.631C>A MANE Select	ENSP00000360107.4:p.Pro211Thr
ENST00000480623.6:c.631C>A	ENSP00000434498.2:p.Pro211Thr
ENST00000635760.1:c.307C>A	ENSP00000489765.1:p.Pro103Thr
ENST00000635812.1:c.631C>A	ENSP00000490859.1:p.Pro211Thr
ENST00000635866.1:c.*500C>A	ENSP00000489866.1:n.*500C>A
ENST00000635911.1:n.892C>A
ENST00000635984.1:c.307C>A	ENSP00000489921.1:p.Pro103Thr
ENST00000635996.1:c.631C>A	ENSP00000490256.1:p.Pro211Thr
ENST00000636107.1:c.631C>A	ENSP00000489680.1:p.Pro211Thr
ENST00000636253.1:n.285C>A
ENST00000636311.1:n.525C>A
ENST00000636343.1:c.297C>A
ENST00000636379.1:c.343C>A	ENSP00000490622.1:p.Pro115Thr
ENST00000636398.1:c.298C>A	ENSP00000489654.1:p.Pro100Thr
ENST00000636489.1:c.574C>A	ENSP00000489998.1:p.Pro192Thr
ENST00000636702.1:c.601C>A	ENSP00000489623.1:p.Pro201Thr
ENST00000636954.1:c.574C>A	ENSP00000489966.1:p.Pro192Thr
ENST00000637089.1:c.631C>A	ENSP00000489854.1:p.Pro211Thr
ENST00000637200.1:c.*647C>A	ENSP00000490567.1:n.*647C>A
ENST00000637263.1:c.631C>A	ENSP00000489700.1:p.Pro211Thr
ENST00000637340.1:n.1299C>A
ENST00000637353.1:c.631C>A	ENSP00000490441.1:p.Pro211Thr
ENST00000637602.1:c.*332C>A	ENSP00000490074.1:n.*332C>A
ENST00000637849.1:n.695C>A
ENST00000637892.1:n.835C>A
ENST00000638075.1:c.13C>A	ENSP00000490711.1:p.Pro5Thr
ENST00000371068.9:c.631C>A	ENSP00000360107.4:p.Pro211Thr
ENST00000480623.5:c.631C>A	ENSP00000434498.1:p.Pro211Thr
ENST00000538167.2:c.574C>A	ENSP00000444521.1:p.Pro192Thr
NM_001172420.1:c.574C>A	NP_001165891.1:p.Pro192Thr
NM_018100.3:c.631C>A	NP_060570.2:p.Pro211Thr
NR_033327.1:n.846C>A
NM_018100.4:c.631C>A MANE Select	NP_060570.2:p.Pro211Thr
NM_001172420.2:c.574C>A	NP_001165891.1:p.Pro192Thr
NR_033327.2:n.700C>A