Canonical Allele Identifier: CA2577164116

Gene: CHN1

Linked Data

• gnomAD v4: 2-174811470-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174811470G>T , CM000664.2:g.174811470G>T	GRCh38
NC_000002.11:g.175676198G>T , CM000664.1:g.175676198G>T	GRCh37
NC_000002.10:g.175384444G>T	NCBI36
NG_012642.1:g.198973C>A
NG_012642.2:g.198973C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295497.13:c.589+41C>A	ENSP00000295497.7:n.589+41C>A
ENST00000444394.7:c.589+41C>A	ENSP00000411911.2:n.589+41C>A
ENST00000295497.12:c.589+41C>A	ENSP00000295497.7:n.589+41C>A
ENST00000409089.7:c.340+41C>A	ENSP00000386322.3:n.340+41C>A
ENST00000409900.9:c.964+41C>A MANE Select	ENSP00000386741.4:n.964+41C>A
ENST00000413882.6:c.418+41C>A	ENSP00000410496.2:n.418+41C>A
ENST00000443238.6:c.442+41C>A	ENSP00000409798.2:n.442+41C>A
ENST00000444394.6:c.589+41C>A	ENSP00000411911.2:n.589+41C>A
ENST00000488080.6:n.607+41C>A
ENST00000650731.1:c.289+41C>A	ENSP00000499146.1:n.289+41C>A
ENST00000650938.1:c.488+41C>A
ENST00000651246.1:c.556+41C>A	ENSP00000498484.1:n.556+41C>A
ENST00000651501.1:c.*411+41C>A	ENSP00000498894.1:n.*411+41C>A
ENST00000651717.1:c.*240+41C>A	ENSP00000499124.1:n.*240+41C>A
ENST00000652036.1:c.640+41C>A	ENSP00000499139.1:n.640+41C>A
ENST00000295497.11:c.589+41C>A	ENSP00000295497.7:n.589+41C>A
ENST00000409089.6:c.340+41C>A	ENSP00000386322.2:n.340+41C>A
ENST00000409156.7:c.886+41C>A	ENSP00000386470.3:n.886+41C>A
ENST00000409597.5:c.412+41C>A	ENSP00000386469.1:n.412+41C>A
ENST00000409900.7:c.964+41C>A	ENSP00000386741.3:n.964+41C>A
ENST00000413882.5:c.418+41C>A	ENSP00000410496.1:n.418+41C>A
ENST00000443238.5:c.442+41C>A	ENSP00000409798.1:n.442+41C>A
ENST00000444394.5:c.289+41C>A	ENSP00000411911.1:n.289+41C>A
ENST00000488080.5:n.815+41C>A
ENST00000491801.1:n.164C>A
NM_001025201.3:c.886+41C>A	NP_001020372.2:n.886+41C>A
NM_001206602.1:c.589+41C>A	NP_001193531.1:n.589+41C>A
NM_001822.5:c.964+41C>A	NP_001813.1:n.964+41C>A
NR_038133.1:n.830+41C>A
NM_001025201.4:c.886+41C>A	NP_001020372.2:n.886+41C>A
NM_001206602.2:c.589+41C>A	NP_001193531.1:n.589+41C>A
NM_001371513.1:c.964+41C>A	NP_001358442.1:n.964+41C>A
NM_001371514.1:c.1015+41C>A	NP_001358443.1:n.1015+41C>A
NM_001822.7:c.964+41C>A MANE Select	NP_001813.1:n.964+41C>A
NR_038133.2:n.832+41C>A