Canonical Allele Identifier: CA760990782

Gene: CHN1

Linked Data

• dbSNP Id: rs1224117180
• MyVariant Identifiers: chr2:g.175664819T>C (hg19) ; chr2:g.174800091T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174800091T>C , CM000664.2:g.174800091T>C	GRCh38
NC_000002.11:g.175664819T>C , CM000664.1:g.175664819T>C	GRCh37
NC_000002.10:g.175373065T>C	NCBI36
NG_012642.1:g.210352A>G
NG_012642.2:g.210352A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.*25A>G	ENSP00000295497.7:n.*25A>G
ENST00000295497.12:c.*25A>G	ENSP00000295497.7:n.*25A>G
ENST00000409900.9:c.*25A>G MANE Select	ENSP00000386741.4:n.*25A>G
ENST00000413882.6:c.*25A>G	ENSP00000410496.2:n.*25A>G
ENST00000443238.6:c.*25A>G	ENSP00000409798.2:n.*25A>G
ENST00000488080.6:n.1048A>G
ENST00000650731.1:c.*25A>G	ENSP00000499146.1:n.*25A>G
ENST00000650938.1:c.791A>G
ENST00000651246.1:c.*25A>G	ENSP00000498484.1:n.*25A>G
ENST00000651501.1:c.*852A>G	ENSP00000498894.1:n.*852A>G
ENST00000651717.1:c.*681A>G	ENSP00000499124.1:n.*681A>G
ENST00000652036.1:c.*25A>G	ENSP00000499139.1:n.*25A>G
ENST00000295497.11:c.*25A>G	ENSP00000295497.7:n.*25A>G
ENST00000409156.7:c.*25A>G	ENSP00000386470.3:n.*25A>G
ENST00000409597.5:c.*25A>G	ENSP00000386469.1:n.*25A>G
ENST00000409900.7:c.*25A>G	ENSP00000386741.3:n.*25A>G
ENST00000488080.5:n.1256A>G
ENST00000492964.1:n.548A>G
NM_001025201.3:c.*25A>G	NP_001020372.2:n.*25A>G
NM_001206602.1:c.*25A>G	NP_001193531.1:n.*25A>G
NM_001822.5:c.*25A>G	NP_001813.1:n.*25A>G
NR_038133.1:n.1271A>G
NM_001025201.4:c.*25A>G	NP_001020372.2:n.*25A>G
NM_001206602.2:c.*25A>G	NP_001193531.1:n.*25A>G
NM_001371513.1:c.*25A>G	NP_001358442.1:n.*25A>G
NM_001371514.1:c.*25A>G	NP_001358443.1:n.*25A>G
NM_001822.7:c.*25A>G MANE Select	NP_001813.1:n.*25A>G
NR_038133.2:n.1273A>G