Canonical Allele Identifier: CA450427239

Gene: EFHC1

Linked Data

• gnomAD v4: 6-52479042-C-T
• COSMIC: COSM3628509
• MyVariant Identifiers: chr6:g.52343840C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479042C>T , CM000668.2:g.52479042C>T	GRCh38
NC_000006.11:g.52343840C>T , CM000668.1:g.52343840C>T	GRCh37
NC_000006.10:g.52451799C>T	NCBI36
NG_016760.1:g.63847C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1284C>T MANE Select	ENSP00000360107.4:p.Ser428=
ENST00000480623.6:c.1284C>T	ENSP00000434498.2:p.Ser428=
ENST00000635760.1:c.960C>T	ENSP00000489765.1:p.Ser320=
ENST00000635812.1:c.*585C>T	ENSP00000490859.1:n.*585C>T
ENST00000635866.1:c.*1153C>T	ENSP00000489866.1:n.*1153C>T
ENST00000635911.1:n.2802C>T
ENST00000635984.1:c.960C>T	ENSP00000489921.1:p.Ser320=
ENST00000635996.1:c.1284C>T	ENSP00000490256.1:p.Ser428=
ENST00000636107.1:c.1284C>T	ENSP00000489680.1:p.Ser428=
ENST00000636311.1:n.1178C>T
ENST00000636343.1:c.950C>T
ENST00000636379.1:c.996C>T	ENSP00000490622.1:p.Ser332=
ENST00000636398.1:c.984C>T	ENSP00000489654.1:n.984C>T
ENST00000636489.1:c.1227C>T	ENSP00000489998.1:p.Ser409=
ENST00000636616.1:n.895-50C>T
ENST00000636702.1:c.1254C>T	ENSP00000489623.1:p.Ser418=
ENST00000636954.1:c.1227C>T	ENSP00000489966.1:p.Ser409=
ENST00000637089.1:c.1284C>T	ENSP00000489854.1:p.Ser428=
ENST00000637121.1:n.1086C>T
ENST00000637263.1:c.1284C>T	ENSP00000489700.1:p.Ser428=
ENST00000637340.1:n.3209C>T
ENST00000637353.1:c.1284C>T	ENSP00000490441.1:p.Ser428=
ENST00000637602.1:c.*985C>T	ENSP00000490074.1:n.*985C>T
ENST00000637849.1:n.1348C>T
ENST00000637874.1:c.229C>T	ENSP00000490348.1:n.229C>T
ENST00000637892.1:n.1488C>T
ENST00000371068.9:c.1284C>T	ENSP00000360107.4:p.Ser428=
ENST00000480623.5:c.*1704C>T	ENSP00000434498.1:n.*1704C>T
ENST00000538167.2:c.1227C>T	ENSP00000444521.1:p.Ser409=
NM_001172420.1:c.1227C>T	NP_001165891.1:p.Ser409=
NM_018100.3:c.1284C>T	NP_060570.2:p.Ser428=
NR_033327.1:n.2756C>T
NM_018100.4:c.1284C>T MANE Select	NP_060570.2:p.Ser428=
NM_001172420.2:c.1227C>T	NP_001165891.1:p.Ser409=
NR_033327.2:n.2610C>T