Canonical Allele Identifier: CA2753244809

Gene: CHN1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799962_174799963insA , CM000664.2:g.174799962_174799963insA	GRCh38
NC_000002.11:g.175664690_175664691insA , CM000664.1:g.175664690_175664691insA	GRCh37
NC_000002.10:g.175372936_175372937insA	NCBI36
NG_012642.1:g.210480_210481insT
NG_012642.2:g.210480_210481insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*153_*154insT	ENSP00000295497.7:n.*153_*154insT
ENST00000295497.12:c.*153_*154insT	ENSP00000295497.7:n.*153_*154insT
ENST00000409900.9:c.*153_*154insT MANE Select	ENSP00000386741.4:n.*153_*154insT
ENST00000413882.6:c.*153_*154insT	ENSP00000410496.2:n.*153_*154insT
ENST00000443238.6:c.*153_*154insT	ENSP00000409798.2:n.*153_*154insT
ENST00000488080.6:n.1176_1177insT
ENST00000650731.1:c.*153_*154insT	ENSP00000499146.1:n.*153_*154insT
ENST00000650938.1:c.919_920insT
ENST00000651246.1:c.*153_*154insT	ENSP00000498484.1:n.*153_*154insT
ENST00000651501.1:c.*980_*981insT	ENSP00000498894.1:n.*980_*981insT
ENST00000651717.1:c.*809_*810insT	ENSP00000499124.1:n.*809_*810insT
ENST00000652036.1:c.*153_*154insT	ENSP00000499139.1:n.*153_*154insT
ENST00000295497.11:c.*153_*154insT	ENSP00000295497.7:n.*153_*154insT
ENST00000409597.5:c.*153_*154insT	ENSP00000386469.1:n.*153_*154insT
ENST00000409900.7:c.*153_*154insT	ENSP00000386741.3:n.*153_*154insT
ENST00000488080.5:n.1384_1385insT
ENST00000492964.1:n.676_677insT
NM_001025201.3:c.*153_*154insT	NP_001020372.2:n.*153_*154insT
NM_001206602.1:c.*153_*154insT	NP_001193531.1:n.*153_*154insT
NM_001822.5:c.*153_*154insT	NP_001813.1:n.*153_*154insT
NR_038133.1:n.1399_1400insT
NM_001025201.4:c.*153_*154insT	NP_001020372.2:n.*153_*154insT
NM_001206602.2:c.*153_*154insT	NP_001193531.1:n.*153_*154insT
NM_001371513.1:c.*153_*154insT	NP_001358442.1:n.*153_*154insT
NM_001371514.1:c.*153_*154insT	NP_001358443.1:n.*153_*154insT
NM_001822.7:c.*153_*154insT MANE Select	NP_001813.1:n.*153_*154insT
NR_038133.2:n.1401_1402insT