Canonical Allele Identifier: CA355456436

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184075628A>G (hg19) ; chr3:g.184357840A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184357840A>G , CM000665.2:g.184357840A>G	GRCh38
NC_000003.11:g.184075628A>G , CM000665.1:g.184075628A>G	GRCh37
NC_000003.10:g.185558322A>G	NCBI36
NG_016422.1:g.8764T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265593.9:c.632T>C (CLCN2) MANE Select	ENSP00000265593.4:p.Ile211Thr
ENST00000475279.2:c.88+122T>C (CLCN2)
ENST00000636180.1:c.615+122T>C (CLCN2)	ENSP00000490374.1:n.615+122T>C
ENST00000636241.1:c.584+122T>C (CLCN2)
ENST00000636492.1:c.515T>C (CLCN2)	ENSP00000490313.1:p.Ile172Thr
ENST00000636661.1:c.615+122T>C (CLCN2)	ENSP00000490764.1:n.615+122T>C
ENST00000637392.1:n.591+122T>C (CLCN2)
ENST00000637909.1:c.340T>C (CLCN2)
ENST00000638134.1:c.580+122T>C (CLCN2)
ENST00000265593.8:c.632T>C (CLCN2)	ENSP00000265593.4:p.Ile211Thr
ENST00000344937.11:c.632T>C (CLCN2)	ENSP00000345056.7:p.Ile211Thr
ENST00000434054.6:c.500T>C (CLCN2)	ENSP00000400425.2:p.Ile167Thr
ENST00000444495.1:c.2106+213133A>G (EIF2B5)	ENSP00000409142.1:n.2106+213133A>G
ENST00000457512.1:c.632T>C (CLCN2)	ENSP00000391928.1:p.Ile211Thr
ENST00000485667.1:n.639T>C (CLCN2)
NM_001171087.2:c.632T>C (CLCN2)	NP_001164558.1:p.Ile211Thr
NM_001171088.2:c.500T>C (CLCN2)	NP_001164559.1:p.Ile167Thr
NM_001171089.2:c.632T>C (CLCN2)	NP_001164560.1:p.Ile211Thr
NM_004366.5:c.632T>C (CLCN2)	NP_004357.3:p.Ile211Thr
XM_006713489.1:c.632T>C (CLCN2)	XP_006713552.1:p.Ile211Thr
XM_011512401.1:c.632T>C (CLCN2)	XP_011510703.1:p.Ile211Thr
XM_011512402.1:c.632T>C (CLCN2)	XP_011510704.1:p.Ile211Thr
XM_006713490.2:c.-453+122T>C (CLCN2)	XP_006713553.1:n.-453+122T>C
XR_001740001.1:n.756T>C (CLCN2)
XR_001740002.1:n.756T>C (CLCN2)
NM_004366.6:c.632T>C (CLCN2) MANE Select	NP_004357.3:p.Ile211Thr
NM_001171087.3:c.632T>C (CLCN2)	NP_001164558.1:p.Ile211Thr
NM_001171088.3:c.500T>C (CLCN2)	NP_001164559.1:p.Ile167Thr
NM_001171089.3:c.632T>C (CLCN2)	NP_001164560.1:p.Ile211Thr