Canonical Allele Identifier: CA349347806

Gene: CHN1

Linked Data

• MyVariant Identifiers: chr2:g.175689204T>C (hg19) ; chr2:g.174824476T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824476T>C , CM000664.2:g.174824476T>C	GRCh38
NC_000002.11:g.175689204T>C , CM000664.1:g.175689204T>C	GRCh37
NC_000002.10:g.175397450T>C	NCBI36
NG_012642.1:g.185967A>G
NG_012642.2:g.185967A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.295A>G	ENSP00000295497.7:p.Asn99Asp
ENST00000444394.7:c.295A>G	ENSP00000411911.2:p.Asn99Asp
ENST00000295497.12:c.295A>G	ENSP00000295497.7:p.Asn99Asp
ENST00000409089.7:c.-6A>G	ENSP00000386322.3:n.-6A>G
ENST00000409900.9:c.670A>G MANE Select	ENSP00000386741.4:p.Asn224Asp
ENST00000413882.6:c.124A>G	ENSP00000410496.2:p.Asn42Asp
ENST00000425395.6:c.*117A>G	ENSP00000405270.2:n.*117A>G
ENST00000443238.6:c.148A>G	ENSP00000409798.2:p.Asn50Asp
ENST00000444394.6:c.295A>G	ENSP00000411911.2:p.Asn99Asp
ENST00000444573.2:c.514A>G	ENSP00000392603.2:p.Asn172Asp
ENST00000488080.6:n.313A>G
ENST00000650731.1:c.-6A>G	ENSP00000499146.1:n.-6A>G
ENST00000650938.1:c.194A>G
ENST00000651246.1:c.262A>G	ENSP00000498484.1:p.Asn88Asp
ENST00000651373.1:c.184A>G	ENSP00000499174.1:p.Asn62Asp
ENST00000651501.1:c.*117A>G	ENSP00000498894.1:n.*117A>G
ENST00000651717.1:c.253-11994A>G	ENSP00000499124.1:n.253-11994A>G
ENST00000652036.1:c.295A>G	ENSP00000499139.1:p.Asn99Asp
ENST00000652154.1:n.568A>G
ENST00000295497.11:c.295A>G	ENSP00000295497.7:p.Asn99Asp
ENST00000409089.6:c.-6A>G	ENSP00000386322.2:n.-6A>G
ENST00000409156.7:c.592A>G	ENSP00000386470.3:p.Asn198Asp
ENST00000409597.5:c.118A>G	ENSP00000386469.1:p.Asn40Asp
ENST00000409900.7:c.670A>G	ENSP00000386741.3:p.Asn224Asp
ENST00000413882.5:c.124A>G	ENSP00000410496.1:p.Asn42Asp
ENST00000425395.5:c.*221A>G	ENSP00000405270.1:n.*221A>G
ENST00000443238.5:c.148A>G	ENSP00000409798.1:p.Asn50Asp
ENST00000444394.5:c.-6A>G	ENSP00000411911.1:n.-6A>G
ENST00000444573.1:c.295A>G	ENSP00000392603.1:p.Asn99Asp
ENST00000485882.1:n.129A>G
ENST00000488080.5:n.521A>G
NM_001025201.3:c.592A>G	NP_001020372.2:p.Asn198Asp
NM_001206602.1:c.295A>G	NP_001193531.1:p.Asn99Asp
NM_001822.5:c.670A>G	NP_001813.1:p.Asn224Asp
NR_038133.1:n.536A>G
NM_001025201.4:c.592A>G	NP_001020372.2:p.Asn198Asp
NM_001206602.2:c.295A>G	NP_001193531.1:p.Asn99Asp
NM_001371513.1:c.670A>G	NP_001358442.1:p.Asn224Asp
NM_001371514.1:c.721A>G	NP_001358443.1:p.Asn241Asp
NM_001822.7:c.670A>G MANE Select	NP_001813.1:p.Asn224Asp
NR_038133.2:n.538A>G