Canonical Allele Identifier: CA349347840

Gene: CHN1

Linked Data

• MyVariant Identifiers: chr2:g.175689212T>C (hg19) ; chr2:g.174824484T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824484T>C , CM000664.2:g.174824484T>C	GRCh38
NC_000002.11:g.175689212T>C , CM000664.1:g.175689212T>C	GRCh37
NC_000002.10:g.175397458T>C	NCBI36
NG_012642.1:g.185959A>G
NG_012642.2:g.185959A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.287A>G	ENSP00000295497.7:p.Tyr96Cys
ENST00000444394.7:c.287A>G	ENSP00000411911.2:p.Tyr96Cys
ENST00000295497.12:c.287A>G	ENSP00000295497.7:p.Tyr96Cys
ENST00000409089.7:c.-14A>G	ENSP00000386322.3:n.-14A>G
ENST00000409900.9:c.662A>G MANE Select	ENSP00000386741.4:p.Tyr221Cys
ENST00000413882.6:c.116A>G	ENSP00000410496.2:p.Tyr39Cys
ENST00000425395.6:c.*109A>G	ENSP00000405270.2:n.*109A>G
ENST00000443238.6:c.140A>G	ENSP00000409798.2:p.Tyr47Cys
ENST00000444394.6:c.287A>G	ENSP00000411911.2:p.Tyr96Cys
ENST00000444573.2:c.506A>G	ENSP00000392603.2:p.Tyr169Cys
ENST00000488080.6:n.305A>G
ENST00000650731.1:c.-14A>G	ENSP00000499146.1:n.-14A>G
ENST00000650938.1:c.186A>G
ENST00000651246.1:c.254A>G	ENSP00000498484.1:p.Tyr85Cys
ENST00000651373.1:c.176A>G	ENSP00000499174.1:p.Tyr59Cys
ENST00000651501.1:c.*109A>G	ENSP00000498894.1:n.*109A>G
ENST00000651717.1:c.253-12002A>G	ENSP00000499124.1:n.253-12002A>G
ENST00000652036.1:c.287A>G	ENSP00000499139.1:p.Tyr96Cys
ENST00000652154.1:n.560A>G
ENST00000295497.11:c.287A>G	ENSP00000295497.7:p.Tyr96Cys
ENST00000409089.6:c.-14A>G	ENSP00000386322.2:n.-14A>G
ENST00000409156.7:c.584A>G	ENSP00000386470.3:p.Tyr195Cys
ENST00000409597.5:c.110A>G	ENSP00000386469.1:p.Tyr37Cys
ENST00000409900.7:c.662A>G	ENSP00000386741.3:p.Tyr221Cys
ENST00000413882.5:c.116A>G	ENSP00000410496.1:p.Tyr39Cys
ENST00000425395.5:c.*213A>G	ENSP00000405270.1:n.*213A>G
ENST00000443238.5:c.140A>G	ENSP00000409798.1:p.Tyr47Cys
ENST00000444394.5:c.-14A>G	ENSP00000411911.1:n.-14A>G
ENST00000444573.1:c.287A>G	ENSP00000392603.1:p.Tyr96Cys
ENST00000485882.1:n.121A>G
ENST00000488080.5:n.513A>G
NM_001025201.3:c.584A>G	NP_001020372.2:p.Tyr195Cys
NM_001206602.1:c.287A>G	NP_001193531.1:p.Tyr96Cys
NM_001822.5:c.662A>G	NP_001813.1:p.Tyr221Cys
NR_038133.1:n.528A>G
NM_001025201.4:c.584A>G	NP_001020372.2:p.Tyr195Cys
NM_001206602.2:c.287A>G	NP_001193531.1:p.Tyr96Cys
NM_001371513.1:c.662A>G	NP_001358442.1:p.Tyr221Cys
NM_001371514.1:c.713A>G	NP_001358443.1:p.Tyr238Cys
NM_001822.7:c.662A>G MANE Select	NP_001813.1:p.Tyr221Cys
NR_038133.2:n.530A>G