Canonical Allele Identifier: CA2679104496

Gene: EFHC1

Linked Data

• gnomAD v4: 6-52479977-T-TGACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.52479977_52479978insGACCC , CM000668.2:g.52479977_52479978insGACCC	GRCh38
NC_000006.11:g.52344775_52344776insGACCC , CM000668.1:g.52344775_52344776insGACCC	GRCh37
NC_000006.10:g.52452734_52452735insGACCC	NCBI36
NG_016760.1:g.64782_64783insGACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371068.11:c.1640+190_1640+191insGACCC MANE Select	ENSP00000360107.4:n.1640+190_1640+191insGACCC
ENST00000480623.6:c.1640+190_1640+191insGACCC	ENSP00000434498.2:n.1640+190_1640+191insGACCC
ENST00000635760.1:c.1316+190_1316+191insGACCC	ENSP00000489765.1:n.1316+190_1316+191insGACCC
ENST00000635812.1:c.*941+190_*941+191insGACCC	ENSP00000490859.1:n.*941+190_*941+191insGACCC
ENST00000635866.1:c.*1509+190_*1509+191insGACCC	ENSP00000489866.1:n.*1509+190_*1509+191insGACCC
ENST00000635911.1:n.3158+190_3158+191insGACCC
ENST00000635984.1:c.1316+190_1316+191insGACCC	ENSP00000489921.1:n.1316+190_1316+191insGACCC
ENST00000635996.1:c.1640+190_1640+191insGACCC	ENSP00000490256.1:n.1640+190_1640+191insGACCC
ENST00000636107.1:c.1640+190_1640+191insGACCC	ENSP00000489680.1:n.1640+190_1640+191insGACCC
ENST00000636311.1:n.1534+190_1534+191insGACCC
ENST00000636343.1:c.1306+190_1306+191insGACCC
ENST00000636379.1:c.1352+190_1352+191insGACCC	ENSP00000490622.1:n.1352+190_1352+191insGACCC
ENST00000636398.1:c.1340+190_1340+191insGACCC	ENSP00000489654.1:n.1340+190_1340+191insGACCC
ENST00000636489.1:c.1583+190_1583+191insGACCC	ENSP00000489998.1:n.1583+190_1583+191insGACCC
ENST00000636616.1:n.1201+190_1201+191insGACCC
ENST00000636702.1:c.1610+190_1610+191insGACCC	ENSP00000489623.1:n.1610+190_1610+191insGACCC
ENST00000636954.1:c.1583+190_1583+191insGACCC	ENSP00000489966.1:n.1583+190_1583+191insGACCC
ENST00000637089.1:c.1640+190_1640+191insGACCC	ENSP00000489854.1:n.1640+190_1640+191insGACCC
ENST00000637121.1:n.1442+190_1442+191insGACCC
ENST00000637263.1:c.*171_*172insGACCC	ENSP00000489700.1:n.*171_*172insGACCC
ENST00000637340.1:n.3565+190_3565+191insGACCC
ENST00000637353.1:c.1640+190_1640+191insGACCC	ENSP00000490441.1:n.1640+190_1640+191insGACCC
ENST00000637602.1:c.*1341+190_*1341+191insGACCC	ENSP00000490074.1:n.*1341+190_*1341+191insGACCC
ENST00000637849.1:n.1704+190_1704+191insGACCC
ENST00000637892.1:n.1844+190_1844+191insGACCC
ENST00000371068.9:c.1640+190_1640+191insGACCC	ENSP00000360107.4:n.1640+190_1640+191insGACCC
ENST00000480623.5:c.*2060+190_*2060+191insGACCC	ENSP00000434498.1:n.*2060+190_*2060+191insGACCC
ENST00000538167.2:c.1583+190_1583+191insGACCC	ENSP00000444521.1:n.1583+190_1583+191insGACCC
NM_001172420.1:c.1583+190_1583+191insGACCC	NP_001165891.1:n.1583+190_1583+191insGACCC
NM_018100.3:c.1640+190_1640+191insGACCC	NP_060570.2:n.1640+190_1640+191insGACCC
NR_033327.1:n.3112+190_3112+191insGACCC
NM_018100.4:c.1640+190_1640+191insGACCC MANE Select	NP_060570.2:n.1640+190_1640+191insGACCC
NM_001172420.2:c.1583+190_1583+191insGACCC	NP_001165891.1:n.1583+190_1583+191insGACCC
NR_033327.2:n.2966+190_2966+191insGACCC