Canonical Allele Identifier: CA1308865671

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174824387A= , CM000664.2:g.174824387A=	GRCh38
NC_000002.11:g.175689115A= , CM000664.1:g.175689115A=	GRCh37
NC_000002.10:g.175397361A=	NCBI36
NG_012642.1:g.186056T=
NG_012642.2:g.186056T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.337+47T=	ENSP00000295497.7:n.337+47T=
ENST00000444394.7:c.337+47T=	ENSP00000411911.2:n.337+47T=
ENST00000295497.12:c.337+47T=	ENSP00000295497.7:n.337+47T=
ENST00000409089.7:c.37+47T=	ENSP00000386322.3:n.37+47T=
ENST00000409900.9:c.712+47T= MANE Select	ENSP00000386741.4:n.712+47T=
ENST00000413882.6:c.166+47T=	ENSP00000410496.2:n.166+47T=
ENST00000425395.6:c.*159+47T=	ENSP00000405270.2:n.*159+47T=
ENST00000443238.6:c.190+47T=	ENSP00000409798.2:n.190+47T=
ENST00000444394.6:c.337+47T=	ENSP00000411911.2:n.337+47T=
ENST00000444573.2:c.556+47T=	ENSP00000392603.2:n.556+47T=
ENST00000488080.6:n.355+47T=
ENST00000650731.1:c.37+47T=	ENSP00000499146.1:n.37+47T=
ENST00000650938.1:c.236+47T=
ENST00000651246.1:c.304+47T=	ENSP00000498484.1:n.304+47T=
ENST00000651373.1:c.226+47T=	ENSP00000499174.1:n.226+47T=
ENST00000651501.1:c.*159+47T=	ENSP00000498894.1:n.*159+47T=
ENST00000651717.1:c.253-11905T=	ENSP00000499124.1:n.253-11905T=
ENST00000652036.1:c.337+47T=	ENSP00000499139.1:n.337+47T=
ENST00000652154.1:n.610+47T=
ENST00000295497.11:c.337+47T=	ENSP00000295497.7:n.337+47T=
ENST00000409089.6:c.37+47T=	ENSP00000386322.2:n.37+47T=
ENST00000409156.7:c.634+47T=	ENSP00000386470.3:n.634+47T=
ENST00000409597.5:c.160+47T=	ENSP00000386469.1:n.160+47T=
ENST00000409900.7:c.712+47T=	ENSP00000386741.3:n.712+47T=
ENST00000413882.5:c.166+47T=	ENSP00000410496.1:n.166+47T=
ENST00000425395.5:c.*263+47T=	ENSP00000405270.1:n.*263+47T=
ENST00000443238.5:c.190+47T=	ENSP00000409798.1:n.190+47T=
ENST00000444394.5:c.37+47T=	ENSP00000411911.1:n.37+47T=
ENST00000444573.1:c.337+47T=	ENSP00000392603.1:n.337+47T=
ENST00000485882.1:n.171+47T=
ENST00000488080.5:n.563+47T=
NM_001025201.3:c.634+47T=	NP_001020372.2:n.634+47T=
NM_001206602.1:c.337+47T=	NP_001193531.1:n.337+47T=
NM_001822.5:c.712+47T=	NP_001813.1:n.712+47T=
NR_038133.1:n.578+47T=
NM_001025201.4:c.634+47T=	NP_001020372.2:n.634+47T=
NM_001206602.2:c.337+47T=	NP_001193531.1:n.337+47T=
NM_001371513.1:c.712+47T=	NP_001358442.1:n.712+47T=
NM_001371514.1:c.763+47T=	NP_001358443.1:n.763+47T=
NM_001822.7:c.712+47T= MANE Select	NP_001813.1:n.712+47T=
NR_038133.2:n.580+47T=