Canonical Allele Identifier: CA2668842746

Gene: CLCN2 EIF2B5

Linked Data

• gnomAD v4: 3-184355620-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184355620_184355621insT , CM000665.2:g.184355620_184355621insT	GRCh38
NC_000003.11:g.184073408_184073409insT , CM000665.1:g.184073408_184073409insT	GRCh37
NC_000003.10:g.185556102_185556103insT	NCBI36
NG_016422.1:g.10983_10984insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.1170+73_1170+74insA (CLCN2) MANE Select	ENSP00000265593.4:n.1170+73_1170+74insA
ENST00000475279.2:c.552+73_552+74insA (CLCN2)
ENST00000636180.1:c.*146+73_*146+74insA (CLCN2)	ENSP00000490374.1:n.*146+73_*146+74insA
ENST00000636241.1:c.1061+73_1061+74insA (CLCN2)
ENST00000636492.1:c.1053+73_1053+74insA (CLCN2)	ENSP00000490313.1:n.1053+73_1053+74insA
ENST00000636658.1:c.431+73_431+74insA (CLCN2)
ENST00000636661.1:c.*1360+73_*1360+74insA (CLCN2)	ENSP00000490764.1:n.*1360+73_*1360+74insA
ENST00000637392.1:n.2355_2356insA (CLCN2)
ENST00000637538.1:c.476+73_476+74insA (CLCN2)
ENST00000637909.1:c.976+73_976+74insA (CLCN2)
ENST00000638134.1:c.978+73_978+74insA (CLCN2)
ENST00000265593.8:c.1170+73_1170+74insA (CLCN2)	ENSP00000265593.4:n.1170+73_1170+74insA
ENST00000344937.11:c.1170+73_1170+74insA (CLCN2)	ENSP00000345056.7:n.1170+73_1170+74insA
ENST00000430397.5:c.113+73_113+74insA (CLCN2)
ENST00000434054.6:c.1038+73_1038+74insA (CLCN2)	ENSP00000400425.2:n.1038+73_1038+74insA
ENST00000444495.1:c.2106+210913_2106+210914insT (EIF2B5)	ENSP00000409142.1:n.2106+210913_2106+210914insT
ENST00000457512.1:c.1170+73_1170+74insA (CLCN2)	ENSP00000391928.1:n.1170+73_1170+74insA
ENST00000475279.1:n.188+73_188+74insA (CLCN2)
ENST00000485667.1:n.1177+73_1177+74insA (CLCN2)
NM_001171087.2:c.1170+73_1170+74insA (CLCN2)	NP_001164558.1:n.1170+73_1170+74insA
NM_001171088.2:c.1038+73_1038+74insA (CLCN2)	NP_001164559.1:n.1038+73_1038+74insA
NM_001171089.2:c.1170+73_1170+74insA (CLCN2)	NP_001164560.1:n.1170+73_1170+74insA
NM_004366.5:c.1170+73_1170+74insA (CLCN2)	NP_004357.3:n.1170+73_1170+74insA
XM_006713489.1:c.1170+73_1170+74insA (CLCN2)	XP_006713552.1:n.1170+73_1170+74insA
XM_006713490.1:c.12+73_12+74insA (CLCN2)	XP_006713553.1:n.12+73_12+74insA
XM_011512401.1:c.1170+73_1170+74insA (CLCN2)	XP_011510703.1:n.1170+73_1170+74insA
XM_011512402.1:c.1170+73_1170+74insA (CLCN2)	XP_011510704.1:n.1170+73_1170+74insA
XM_006713490.2:c.12+73_12+74insA (CLCN2)	XP_006713553.1:n.12+73_12+74insA
XR_001740001.1:n.1294+73_1294+74insA (CLCN2)
XR_001740002.1:n.1294+73_1294+74insA (CLCN2)
NM_004366.6:c.1170+73_1170+74insA (CLCN2) MANE Select	NP_004357.3:n.1170+73_1170+74insA
NM_001171087.3:c.1170+73_1170+74insA (CLCN2)	NP_001164558.1:n.1170+73_1170+74insA
NM_001171088.3:c.1038+73_1038+74insA (CLCN2)	NP_001164559.1:n.1038+73_1038+74insA
NM_001171089.3:c.1170+73_1170+74insA (CLCN2)	NP_001164560.1:n.1170+73_1170+74insA