Canonical Allele Identifier: CA760990559

Gene: CHN1

Linked Data

• dbSNP Id: rs1413214288
• gnomAD v3: 2-174799858-TA-T
• gnomAD v4: 2-174799858-TA-T
• MyVariant Identifiers: chr2:g.175664587del (hg19) ; chr2:g.174799859del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.174799859del , CM000664.2:g.174799859del	GRCh38
NC_000002.11:g.175664587del , CM000664.1:g.175664587del	GRCh37
NC_000002.10:g.175372833del	NCBI36
NG_012642.1:g.210584del
NG_012642.2:g.210584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295497.13:c.*257del	ENSP00000295497.7:n.*257del
ENST00000295497.12:c.*257del	ENSP00000295497.7:n.*257del
ENST00000409900.9:c.*257del MANE Select	ENSP00000386741.4:n.*257del
ENST00000413882.6:c.*257del	ENSP00000410496.2:n.*257del
ENST00000443238.6:c.*257del	ENSP00000409798.2:n.*257del
ENST00000488080.6:n.1280del
ENST00000650731.1:c.*257del	ENSP00000499146.1:n.*257del
ENST00000650938.1:c.1023del
ENST00000651246.1:c.*257del	ENSP00000498484.1:n.*257del
ENST00000651501.1:c.*1084del	ENSP00000498894.1:n.*1084del
ENST00000651717.1:c.*913del	ENSP00000499124.1:n.*913del
ENST00000652036.1:c.*257del	ENSP00000499139.1:n.*257del
ENST00000295497.11:c.*257del	ENSP00000295497.7:n.*257del
ENST00000409597.5:c.*257del	ENSP00000386469.1:n.*257del
ENST00000409900.7:c.*257del	ENSP00000386741.3:n.*257del
ENST00000488080.5:n.1488del
NM_001025201.3:c.*257del	NP_001020372.2:n.*257del
NM_001206602.1:c.*257del	NP_001193531.1:n.*257del
NM_001822.5:c.*257del	NP_001813.1:n.*257del
NR_038133.1:n.1503del
NM_001025201.4:c.*257del	NP_001020372.2:n.*257del
NM_001206602.2:c.*257del	NP_001193531.1:n.*257del
NM_001371513.1:c.*257del	NP_001358442.1:n.*257del
NM_001371514.1:c.*257del	NP_001358443.1:n.*257del
NM_001822.7:c.*257del MANE Select	NP_001813.1:n.*257del
NR_038133.2:n.1505del