Canonical Allele Identifier: CA355446937

Gene: CLCN2 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184069847A>T (hg19) ; chr3:g.184352059A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184352059A>T , CM000665.2:g.184352059A>T	GRCh38
NC_000003.11:g.184069847A>T , CM000665.1:g.184069847A>T	GRCh37
NC_000003.10:g.185552541A>T	NCBI36
NG_016422.1:g.14545T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265593.9:c.2369T>A (CLCN2) MANE Select	ENSP00000265593.4:p.Ile790Asn
ENST00000636180.1:c.*1267T>A (CLCN2)	ENSP00000490374.1:n.*1267T>A
ENST00000636661.1:c.*2679T>A (CLCN2)	ENSP00000490764.1:n.*2679T>A
ENST00000637392.1:n.3911T>A (CLCN2)
ENST00000637909.1:c.2175T>A (CLCN2)
ENST00000265593.8:c.2369T>A (CLCN2)	ENSP00000265593.4:p.Ile790Asn
ENST00000344937.11:c.2318T>A (CLCN2)	ENSP00000345056.7:p.Ile773Asn
ENST00000430397.5:c.1177+234T>A (CLCN2)
ENST00000434054.6:c.2237T>A (CLCN2)	ENSP00000400425.2:p.Ile746Asn
ENST00000444495.1:c.2106+207352A>T (EIF2B5)	ENSP00000409142.1:n.2106+207352A>T
ENST00000457512.1:c.2369T>A (CLCN2)	ENSP00000391928.1:p.Ile790Asn
NM_001171087.2:c.2318T>A (CLCN2)	NP_001164558.1:p.Ile773Asn
NM_001171088.2:c.2237T>A (CLCN2)	NP_001164559.1:p.Ile746Asn
NM_001171089.2:c.2369T>A (CLCN2)	NP_001164560.1:p.Ile790Asn
NM_004366.5:c.2369T>A (CLCN2)	NP_004357.3:p.Ile790Asn
XM_006713489.1:c.2310+234T>A (CLCN2)	XP_006713552.1:n.2310+234T>A
XM_006713490.1:c.1211T>A (CLCN2)	XP_006713553.1:p.Ile404Asn
XM_011512401.1:c.2369T>A (CLCN2)	XP_011510703.1:p.Ile790Asn
XM_006713490.2:c.1211T>A (CLCN2)	XP_006713553.1:p.Ile404Asn
XR_001740001.1:n.2549T>A (CLCN2)
XR_001740002.1:n.2490+234T>A (CLCN2)
NM_004366.6:c.2369T>A (CLCN2) MANE Select	NP_004357.3:p.Ile790Asn
NM_001171087.3:c.2318T>A (CLCN2)	NP_001164558.1:p.Ile773Asn
NM_001171088.3:c.2237T>A (CLCN2)	NP_001164559.1:p.Ile746Asn
NM_001171089.3:c.2369T>A (CLCN2)	NP_001164560.1:p.Ile790Asn