Canonical Allele Identifier: CA364458182

Gene: EFHC1

Linked Data

• dbSNP Id: rs1765632669
• gnomAD v3: 6-52479742-A-C
• gnomAD v4: 6-52479742-A-C
• MyVariant Identifiers: chr6:g.52344540A>C (hg19) ; chr6:g.52479742A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479742A>C , CM000668.2:g.52479742A>C	GRCh38
NC_000006.11:g.52344540A>C , CM000668.1:g.52344540A>C	GRCh37
NC_000006.10:g.52452499A>C	NCBI36
NG_016760.1:g.64547A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1595A>C MANE Select	ENSP00000360107.4:p.Gln532Pro
ENST00000480623.6:c.1595A>C	ENSP00000434498.2:p.Gln532Pro
ENST00000635760.1:c.1271A>C	ENSP00000489765.1:p.Gln424Pro
ENST00000635812.1:c.*896A>C	ENSP00000490859.1:n.*896A>C
ENST00000635866.1:c.*1464A>C	ENSP00000489866.1:n.*1464A>C
ENST00000635911.1:n.3113A>C
ENST00000635984.1:c.1271A>C	ENSP00000489921.1:p.Gln424Pro
ENST00000635996.1:c.1595A>C	ENSP00000490256.1:p.Gln532Pro
ENST00000636107.1:c.1595A>C	ENSP00000489680.1:p.Gln532Pro
ENST00000636311.1:n.1489A>C
ENST00000636343.1:c.1261A>C
ENST00000636379.1:c.1307A>C	ENSP00000490622.1:p.Gln436Pro
ENST00000636398.1:c.1295A>C	ENSP00000489654.1:n.1295A>C
ENST00000636489.1:c.1538A>C	ENSP00000489998.1:p.Gln513Pro
ENST00000636616.1:n.1156A>C
ENST00000636702.1:c.1565A>C	ENSP00000489623.1:p.Gln522Pro
ENST00000636954.1:c.1538A>C	ENSP00000489966.1:p.Gln513Pro
ENST00000637089.1:c.1595A>C	ENSP00000489854.1:p.Gln532Pro
ENST00000637121.1:n.1397A>C
ENST00000637263.1:c.1595A>C	ENSP00000489700.1:p.Gln532Pro
ENST00000637340.1:n.3520A>C
ENST00000637353.1:c.1595A>C	ENSP00000490441.1:p.Gln532Pro
ENST00000637602.1:c.*1296A>C	ENSP00000490074.1:n.*1296A>C
ENST00000637849.1:n.1659A>C
ENST00000637892.1:n.1799A>C
ENST00000371068.9:c.1595A>C	ENSP00000360107.4:p.Gln532Pro
ENST00000480623.5:c.*2015A>C	ENSP00000434498.1:n.*2015A>C
ENST00000538167.2:c.1538A>C	ENSP00000444521.1:p.Gln513Pro
NM_001172420.1:c.1538A>C	NP_001165891.1:p.Gln513Pro
NM_018100.3:c.1595A>C	NP_060570.2:p.Gln532Pro
NR_033327.1:n.3067A>C
NM_018100.4:c.1595A>C MANE Select	NP_060570.2:p.Gln532Pro
NM_001172420.2:c.1538A>C	NP_001165891.1:p.Gln513Pro
NR_033327.2:n.2921A>C