Canonical Allele Identifier: CA2753244897
Gene: CHN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.174800429_174800430insACA , CM000664.2:g.174800429_174800430insACA GRCh38
NC_000002.11:g.175665157_175665158insACA , CM000664.1:g.175665157_175665158insACA GRCh37
NC_000002.10:g.175373403_175373404insACA NCBI36
NG_012642.1:g.210013_210014insTGT
NG_012642.2:g.210013_210014insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295497.13:c.834-143_834-142insTGT ENSP00000295497.7:n.834-143_834-142insTGT
ENST00000444394.7:c.963-143_963-142insTGT ENSP00000411911.2:n.963-143_963-142insTGT
ENST00000295497.12:c.834-143_834-142insTGT ENSP00000295497.7:n.834-143_834-142insTGT
ENST00000409089.7:c.585-143_585-142insTGT ENSP00000386322.3:n.585-143_585-142insTGT
ENST00000409900.9:c.1209-143_1209-142insTGT MANE Select ENSP00000386741.4:n.1209-143_1209-142insTGT
ENST00000413882.6:c.663-143_663-142insTGT ENSP00000410496.2:n.663-143_663-142insTGT
ENST00000443238.6:c.687-143_687-142insTGT ENSP00000409798.2:n.687-143_687-142insTGT
ENST00000444394.6:c.963-143_963-142insTGT ENSP00000411911.2:n.963-143_963-142insTGT
ENST00000488080.6:n.852-143_852-142insTGT
ENST00000650731.1:c.534-143_534-142insTGT ENSP00000499146.1:n.534-143_534-142insTGT
ENST00000650938.1:c.595-143_595-142insTGT
ENST00000651246.1:c.801-143_801-142insTGT ENSP00000498484.1:n.801-143_801-142insTGT
ENST00000651501.1:c.*656-143_*656-142insTGT ENSP00000498894.1:n.*656-143_*656-142insTGT
ENST00000651717.1:c.*485-143_*485-142insTGT ENSP00000499124.1:n.*485-143_*485-142insTGT
ENST00000652036.1:c.885-143_885-142insTGT ENSP00000499139.1:n.885-143_885-142insTGT
ENST00000295497.11:c.834-143_834-142insTGT ENSP00000295497.7:n.834-143_834-142insTGT
ENST00000409156.7:c.1131-143_1131-142insTGT ENSP00000386470.3:n.1131-143_1131-142insTGT
ENST00000409597.5:c.657-143_657-142insTGT ENSP00000386469.1:n.657-143_657-142insTGT
ENST00000409900.7:c.1209-143_1209-142insTGT ENSP00000386741.3:n.1209-143_1209-142insTGT
ENST00000488080.5:n.1060-143_1060-142insTGT
ENST00000492964.1:n.352-143_352-142insTGT
NM_001025201.3:c.1131-143_1131-142insTGT NP_001020372.2:n.1131-143_1131-142insTGT
NM_001206602.1:c.834-143_834-142insTGT NP_001193531.1:n.834-143_834-142insTGT
NM_001822.5:c.1209-143_1209-142insTGT NP_001813.1:n.1209-143_1209-142insTGT
NR_038133.1:n.1075-143_1075-142insTGT
NM_001025201.4:c.1131-143_1131-142insTGT NP_001020372.2:n.1131-143_1131-142insTGT
NM_001206602.2:c.834-143_834-142insTGT NP_001193531.1:n.834-143_834-142insTGT
NM_001371513.1:c.1209-143_1209-142insTGT NP_001358442.1:n.1209-143_1209-142insTGT
NM_001371514.1:c.1260-143_1260-142insTGT NP_001358443.1:n.1260-143_1260-142insTGT
NM_001822.7:c.1209-143_1209-142insTGT MANE Select NP_001813.1:n.1209-143_1209-142insTGT
NR_038133.2:n.1077-143_1077-142insTGT