Canonical Allele Identifier: CA1308854550

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799440C= , CM000664.2:g.174799440C=	GRCh38
NC_000002.11:g.175664168C= , CM000664.1:g.175664168C=	GRCh37
NC_000002.10:g.175372414C=	NCBI36
NG_012642.1:g.211003G=
NG_012642.2:g.211003G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*676G=	ENSP00000295497.7:n.*676G=
ENST00000295497.12:c.*676G=	ENSP00000295497.7:n.*676G=
ENST00000409900.9:c.*676G= MANE Select	ENSP00000386741.4:n.*676G=
ENST00000443238.6:c.*676G=	ENSP00000409798.2:n.*676G=
ENST00000652036.1:c.*676G=	ENSP00000499139.1:n.*676G=
ENST00000409900.7:c.*676G=	ENSP00000386741.3:n.*676G=
NM_001025201.3:c.*676G=	NP_001020372.2:n.*676G=
NM_001206602.1:c.*676G=	NP_001193531.1:n.*676G=
NM_001822.5:c.*676G=	NP_001813.1:n.*676G=
NR_038133.1:n.1922G=
NM_001025201.4:c.*676G=	NP_001020372.2:n.*676G=
NM_001206602.2:c.*676G=	NP_001193531.1:n.*676G=
NM_001371513.1:c.*676G=	NP_001358442.1:n.*676G=
NM_001371514.1:c.*676G=	NP_001358443.1:n.*676G=
NM_001822.7:c.*676G= MANE Select	NP_001813.1:n.*676G=
NR_038133.2:n.1924G=