Canonical Allele Identifier: CA1308854592

Gene: CHN1

Linked Data

• dbSNP Id: rs1684646799

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799536G>A , CM000664.2:g.174799536G>A	GRCh38
NC_000002.11:g.175664264G>A , CM000664.1:g.175664264G>A	GRCh37
NC_000002.10:g.175372510G>A	NCBI36
NG_012642.1:g.210907C>T
NG_012642.2:g.210907C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*580C>T	ENSP00000295497.7:n.*580C>T
ENST00000295497.12:c.*580C>T	ENSP00000295497.7:n.*580C>T
ENST00000409900.9:c.*580C>T MANE Select	ENSP00000386741.4:n.*580C>T
ENST00000443238.6:c.*580C>T	ENSP00000409798.2:n.*580C>T
ENST00000488080.6:n.1603C>T
ENST00000650731.1:c.*580C>T	ENSP00000499146.1:n.*580C>T
ENST00000650938.1:c.1346C>T
ENST00000651501.1:c.*1407C>T	ENSP00000498894.1:n.*1407C>T
ENST00000651717.1:c.*1236C>T	ENSP00000499124.1:n.*1236C>T
ENST00000652036.1:c.*580C>T	ENSP00000499139.1:n.*580C>T
ENST00000295497.11:c.*580C>T	ENSP00000295497.7:n.*580C>T
ENST00000409597.5:c.*580C>T	ENSP00000386469.1:n.*580C>T
ENST00000409900.7:c.*580C>T	ENSP00000386741.3:n.*580C>T
ENST00000488080.5:n.1811C>T
NM_001025201.3:c.*580C>T	NP_001020372.2:n.*580C>T
NM_001206602.1:c.*580C>T	NP_001193531.1:n.*580C>T
NM_001822.5:c.*580C>T	NP_001813.1:n.*580C>T
NR_038133.1:n.1826C>T
NM_001025201.4:c.*580C>T	NP_001020372.2:n.*580C>T
NM_001206602.2:c.*580C>T	NP_001193531.1:n.*580C>T
NM_001371513.1:c.*580C>T	NP_001358442.1:n.*580C>T
NM_001371514.1:c.*580C>T	NP_001358443.1:n.*580C>T
NM_001822.7:c.*580C>T MANE Select	NP_001813.1:n.*580C>T
NR_038133.2:n.1828C>T