Canonical Allele Identifier: CA430022750

Gene: CHN1

Linked Data

• MyVariant Identifiers: chr2:g.175689199A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824471A>G , CM000664.2:g.174824471A>G	GRCh38
NC_000002.11:g.175689199A>G , CM000664.1:g.175689199A>G	GRCh37
NC_000002.10:g.175397445A>G	NCBI36
NG_012642.1:g.185972T>C
NG_012642.2:g.185972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.300T>C	ENSP00000295497.7:p.Phe100=
ENST00000444394.7:c.300T>C	ENSP00000411911.2:p.Phe100=
ENST00000295497.12:c.300T>C	ENSP00000295497.7:p.Phe100=
ENST00000409089.7:c.-1T>C	ENSP00000386322.3:n.-1T>C
ENST00000409900.9:c.675T>C MANE Select	ENSP00000386741.4:p.Phe225=
ENST00000413882.6:c.129T>C	ENSP00000410496.2:p.Phe43=
ENST00000425395.6:c.*122T>C	ENSP00000405270.2:n.*122T>C
ENST00000443238.6:c.153T>C	ENSP00000409798.2:p.Phe51=
ENST00000444394.6:c.300T>C	ENSP00000411911.2:p.Phe100=
ENST00000444573.2:c.519T>C	ENSP00000392603.2:p.Phe173=
ENST00000488080.6:n.318T>C
ENST00000650731.1:c.-1T>C	ENSP00000499146.1:n.-1T>C
ENST00000650938.1:c.199T>C
ENST00000651246.1:c.267T>C	ENSP00000498484.1:p.Phe89=
ENST00000651373.1:c.189T>C	ENSP00000499174.1:p.Phe63=
ENST00000651501.1:c.*122T>C	ENSP00000498894.1:n.*122T>C
ENST00000651717.1:c.253-11989T>C	ENSP00000499124.1:n.253-11989T>C
ENST00000652036.1:c.300T>C	ENSP00000499139.1:p.Phe100=
ENST00000652154.1:n.573T>C
ENST00000295497.11:c.300T>C	ENSP00000295497.7:p.Phe100=
ENST00000409089.6:c.-1T>C	ENSP00000386322.2:n.-1T>C
ENST00000409156.7:c.597T>C	ENSP00000386470.3:p.Phe199=
ENST00000409597.5:c.123T>C	ENSP00000386469.1:p.Phe41=
ENST00000409900.7:c.675T>C	ENSP00000386741.3:p.Phe225=
ENST00000413882.5:c.129T>C	ENSP00000410496.1:p.Phe43=
ENST00000425395.5:c.*226T>C	ENSP00000405270.1:n.*226T>C
ENST00000443238.5:c.153T>C	ENSP00000409798.1:p.Phe51=
ENST00000444394.5:c.-1T>C	ENSP00000411911.1:n.-1T>C
ENST00000444573.1:c.300T>C	ENSP00000392603.1:p.Phe100=
ENST00000485882.1:n.134T>C
ENST00000488080.5:n.526T>C
NM_001025201.3:c.597T>C	NP_001020372.2:p.Phe199=
NM_001206602.1:c.300T>C	NP_001193531.1:p.Phe100=
NM_001822.5:c.675T>C	NP_001813.1:p.Phe225=
NR_038133.1:n.541T>C
NM_001025201.4:c.597T>C	NP_001020372.2:p.Phe199=
NM_001206602.2:c.300T>C	NP_001193531.1:p.Phe100=
NM_001371513.1:c.675T>C	NP_001358442.1:p.Phe225=
NM_001371514.1:c.726T>C	NP_001358443.1:p.Phe242=
NM_001822.7:c.675T>C MANE Select	NP_001813.1:p.Phe225=
NR_038133.2:n.543T>C