Canonical Allele Identifier: CA450427471

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52344526A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479728A>G , CM000668.2:g.52479728A>G	GRCh38
NC_000006.11:g.52344526A>G , CM000668.1:g.52344526A>G	GRCh37
NC_000006.10:g.52452485A>G	NCBI36
NG_016760.1:g.64533A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1581A>G MANE Select	ENSP00000360107.4:p.Ala527=
ENST00000480623.6:c.1581A>G	ENSP00000434498.2:p.Ala527=
ENST00000635760.1:c.1257A>G	ENSP00000489765.1:p.Ala419=
ENST00000635812.1:c.*882A>G	ENSP00000490859.1:n.*882A>G
ENST00000635866.1:c.*1450A>G	ENSP00000489866.1:n.*1450A>G
ENST00000635911.1:n.3099A>G
ENST00000635984.1:c.1257A>G	ENSP00000489921.1:p.Ala419=
ENST00000635996.1:c.1581A>G	ENSP00000490256.1:p.Ala527=
ENST00000636107.1:c.1581A>G	ENSP00000489680.1:p.Ala527=
ENST00000636311.1:n.1475A>G
ENST00000636343.1:c.1247A>G
ENST00000636379.1:c.1293A>G	ENSP00000490622.1:p.Ala431=
ENST00000636398.1:c.1281A>G	ENSP00000489654.1:n.1281A>G
ENST00000636489.1:c.1524A>G	ENSP00000489998.1:p.Ala508=
ENST00000636616.1:n.1142A>G
ENST00000636702.1:c.1551A>G	ENSP00000489623.1:p.Ala517=
ENST00000636954.1:c.1524A>G	ENSP00000489966.1:p.Ala508=
ENST00000637089.1:c.1581A>G	ENSP00000489854.1:p.Ala527=
ENST00000637121.1:n.1383A>G
ENST00000637263.1:c.1581A>G	ENSP00000489700.1:p.Ala527=
ENST00000637340.1:n.3506A>G
ENST00000637353.1:c.1581A>G	ENSP00000490441.1:p.Ala527=
ENST00000637602.1:c.*1282A>G	ENSP00000490074.1:n.*1282A>G
ENST00000637849.1:n.1645A>G
ENST00000637892.1:n.1785A>G
ENST00000371068.9:c.1581A>G	ENSP00000360107.4:p.Ala527=
ENST00000480623.5:c.*2001A>G	ENSP00000434498.1:n.*2001A>G
ENST00000538167.2:c.1524A>G	ENSP00000444521.1:p.Ala508=
NM_001172420.1:c.1524A>G	NP_001165891.1:p.Ala508=
NM_018100.3:c.1581A>G	NP_060570.2:p.Ala527=
NR_033327.1:n.3053A>G
NM_018100.4:c.1581A>G MANE Select	NP_060570.2:p.Ala527=
NM_001172420.2:c.1524A>G	NP_001165891.1:p.Ala508=
NR_033327.2:n.2907A>G