Canonical Allele Identifier: CA349347680

Gene: CHN1

Linked Data

• dbSNP Id: rs2105401734
• gnomAD v4: 2-174824442-T-A
• MyVariant Identifiers: chr2:g.175689170T>A (hg19) ; chr2:g.174824442T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824442T>A , CM000664.2:g.174824442T>A	GRCh38
NC_000002.11:g.175689170T>A , CM000664.1:g.175689170T>A	GRCh37
NC_000002.10:g.175397416T>A	NCBI36
NG_012642.1:g.186001A>T
NG_012642.2:g.186001A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.329A>T	ENSP00000295497.7:p.Lys110Ile
ENST00000444394.7:c.329A>T	ENSP00000411911.2:p.Lys110Ile
ENST00000295497.12:c.329A>T	ENSP00000295497.7:p.Lys110Ile
ENST00000409089.7:c.29A>T	ENSP00000386322.3:p.Lys10Ile
ENST00000409900.9:c.704A>T MANE Select	ENSP00000386741.4:p.Lys235Ile
ENST00000413882.6:c.158A>T	ENSP00000410496.2:p.Lys53Ile
ENST00000425395.6:c.*151A>T	ENSP00000405270.2:n.*151A>T
ENST00000443238.6:c.182A>T	ENSP00000409798.2:p.Lys61Ile
ENST00000444394.6:c.329A>T	ENSP00000411911.2:p.Lys110Ile
ENST00000444573.2:c.548A>T	ENSP00000392603.2:p.Lys183Ile
ENST00000488080.6:n.347A>T
ENST00000650731.1:c.29A>T	ENSP00000499146.1:p.Lys10Ile
ENST00000650938.1:c.228A>T
ENST00000651246.1:c.296A>T	ENSP00000498484.1:p.Lys99Ile
ENST00000651373.1:c.218A>T	ENSP00000499174.1:p.Lys73Ile
ENST00000651501.1:c.*151A>T	ENSP00000498894.1:n.*151A>T
ENST00000651717.1:c.253-11960A>T	ENSP00000499124.1:n.253-11960A>T
ENST00000652036.1:c.329A>T	ENSP00000499139.1:p.Lys110Ile
ENST00000652154.1:n.602A>T
ENST00000295497.11:c.329A>T	ENSP00000295497.7:p.Lys110Ile
ENST00000409089.6:c.29A>T	ENSP00000386322.2:p.Lys10Ile
ENST00000409156.7:c.626A>T	ENSP00000386470.3:p.Lys209Ile
ENST00000409597.5:c.152A>T	ENSP00000386469.1:p.Lys51Ile
ENST00000409900.7:c.704A>T	ENSP00000386741.3:p.Lys235Ile
ENST00000413882.5:c.158A>T	ENSP00000410496.1:p.Lys53Ile
ENST00000425395.5:c.*255A>T	ENSP00000405270.1:n.*255A>T
ENST00000443238.5:c.182A>T	ENSP00000409798.1:p.Lys61Ile
ENST00000444394.5:c.29A>T	ENSP00000411911.1:p.Lys10Ile
ENST00000444573.1:c.329A>T	ENSP00000392603.1:p.Lys110Ile
ENST00000485882.1:n.163A>T
ENST00000488080.5:n.555A>T
NM_001025201.3:c.626A>T	NP_001020372.2:p.Lys209Ile
NM_001206602.1:c.329A>T	NP_001193531.1:p.Lys110Ile
NM_001822.5:c.704A>T	NP_001813.1:p.Lys235Ile
NR_038133.1:n.570A>T
NM_001025201.4:c.626A>T	NP_001020372.2:p.Lys209Ile
NM_001206602.2:c.329A>T	NP_001193531.1:p.Lys110Ile
NM_001371513.1:c.704A>T	NP_001358442.1:p.Lys235Ile
NM_001371514.1:c.755A>T	NP_001358443.1:p.Lys252Ile
NM_001822.7:c.704A>T MANE Select	NP_001813.1:p.Lys235Ile
NR_038133.2:n.572A>T