Canonical Allele Identifier: CA364457322

Gene: EFHC1

Linked Data

• MyVariant Identifiers: chr6:g.52343938T>C (hg19) ; chr6:g.52479140T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479140T>C , CM000668.2:g.52479140T>C	GRCh38
NC_000006.11:g.52343938T>C , CM000668.1:g.52343938T>C	GRCh37
NC_000006.10:g.52451897T>C	NCBI36
NG_016760.1:g.63945T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1382T>C MANE Select	ENSP00000360107.4:p.Ile461Thr
ENST00000480623.6:c.1382T>C	ENSP00000434498.2:p.Ile461Thr
ENST00000635760.1:c.1058T>C	ENSP00000489765.1:p.Ile353Thr
ENST00000635812.1:c.*683T>C	ENSP00000490859.1:n.*683T>C
ENST00000635866.1:c.*1251T>C	ENSP00000489866.1:n.*1251T>C
ENST00000635911.1:n.2900T>C
ENST00000635984.1:c.1058T>C	ENSP00000489921.1:p.Ile353Thr
ENST00000635996.1:c.1382T>C	ENSP00000490256.1:p.Ile461Thr
ENST00000636107.1:c.1382T>C	ENSP00000489680.1:p.Ile461Thr
ENST00000636311.1:n.1276T>C
ENST00000636343.1:c.1048T>C
ENST00000636379.1:c.1094T>C	ENSP00000490622.1:p.Ile365Thr
ENST00000636398.1:c.1082T>C	ENSP00000489654.1:n.1082T>C
ENST00000636489.1:c.1325T>C	ENSP00000489998.1:p.Ile442Thr
ENST00000636616.1:n.943T>C
ENST00000636702.1:c.1352T>C	ENSP00000489623.1:p.Ile451Thr
ENST00000636954.1:c.1325T>C	ENSP00000489966.1:p.Ile442Thr
ENST00000637089.1:c.1382T>C	ENSP00000489854.1:p.Ile461Thr
ENST00000637121.1:n.1184T>C
ENST00000637263.1:c.1382T>C	ENSP00000489700.1:p.Ile461Thr
ENST00000637340.1:n.3307T>C
ENST00000637353.1:c.1382T>C	ENSP00000490441.1:p.Ile461Thr
ENST00000637602.1:c.*1083T>C	ENSP00000490074.1:n.*1083T>C
ENST00000637849.1:n.1446T>C
ENST00000637874.1:c.327T>C	ENSP00000490348.1:n.327T>C
ENST00000637892.1:n.1586T>C
ENST00000371068.9:c.1382T>C	ENSP00000360107.4:p.Ile461Thr
ENST00000480623.5:c.*1802T>C	ENSP00000434498.1:n.*1802T>C
ENST00000538167.2:c.1325T>C	ENSP00000444521.1:p.Ile442Thr
NM_001172420.1:c.1325T>C	NP_001165891.1:p.Ile442Thr
NM_018100.3:c.1382T>C	NP_060570.2:p.Ile461Thr
NR_033327.1:n.2854T>C
NM_018100.4:c.1382T>C MANE Select	NP_060570.2:p.Ile461Thr
NM_001172420.2:c.1325T>C	NP_001165891.1:p.Ile442Thr
NR_033327.2:n.2708T>C