Canonical Allele Identifier: CA364458264

Gene: EFHC1

Linked Data

• COSMIC: COSM1080251
• MyVariant Identifiers: chr6:g.52344582A>C (hg19) ; chr6:g.52479784A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479784A>C , CM000668.2:g.52479784A>C	GRCh38
NC_000006.11:g.52344582A>C , CM000668.1:g.52344582A>C	GRCh37
NC_000006.10:g.52452541A>C	NCBI36
NG_016760.1:g.64589A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1637A>C MANE Select	ENSP00000360107.4:p.Glu546Ala
ENST00000480623.6:c.1637A>C	ENSP00000434498.2:p.Glu546Ala
ENST00000635760.1:c.1313A>C	ENSP00000489765.1:p.Glu438Ala
ENST00000635812.1:c.*938A>C	ENSP00000490859.1:n.*938A>C
ENST00000635866.1:c.*1506A>C	ENSP00000489866.1:n.*1506A>C
ENST00000635911.1:n.3155A>C
ENST00000635984.1:c.1313A>C	ENSP00000489921.1:p.Glu438Ala
ENST00000635996.1:c.1637A>C	ENSP00000490256.1:p.Glu546Ala
ENST00000636107.1:c.1637A>C	ENSP00000489680.1:p.Glu546Ala
ENST00000636311.1:n.1531A>C
ENST00000636343.1:c.1303A>C
ENST00000636379.1:c.1349A>C	ENSP00000490622.1:p.Glu450Ala
ENST00000636398.1:c.1337A>C	ENSP00000489654.1:n.1337A>C
ENST00000636489.1:c.1580A>C	ENSP00000489998.1:p.Glu527Ala
ENST00000636616.1:n.1198A>C
ENST00000636702.1:c.1607A>C	ENSP00000489623.1:p.Glu536Ala
ENST00000636954.1:c.1580A>C	ENSP00000489966.1:p.Glu527Ala
ENST00000637089.1:c.1637A>C	ENSP00000489854.1:p.Glu546Ala
ENST00000637121.1:n.1439A>C
ENST00000637263.1:c.1637A>C	ENSP00000489700.1:p.Glu546Ala
ENST00000637340.1:n.3562A>C
ENST00000637353.1:c.1637A>C	ENSP00000490441.1:p.Glu546Ala
ENST00000637602.1:c.*1338A>C	ENSP00000490074.1:n.*1338A>C
ENST00000637849.1:n.1701A>C
ENST00000637892.1:n.1841A>C
ENST00000371068.9:c.1637A>C	ENSP00000360107.4:p.Glu546Ala
ENST00000480623.5:c.*2057A>C	ENSP00000434498.1:n.*2057A>C
ENST00000538167.2:c.1580A>C	ENSP00000444521.1:p.Glu527Ala
NM_001172420.1:c.1580A>C	NP_001165891.1:p.Glu527Ala
NM_018100.3:c.1637A>C	NP_060570.2:p.Glu546Ala
NR_033327.1:n.3109A>C
NM_018100.4:c.1637A>C MANE Select	NP_060570.2:p.Glu546Ala
NM_001172420.2:c.1580A>C	NP_001165891.1:p.Glu527Ala
NR_033327.2:n.2963A>C