Canonical Allele Identifier: CA2663623422
Gene: CHRNG HGNC NCBI

Linked Data

gnomAD v4: 2-232541475-CTA-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232541477_232541478del , CM000664.2:g.232541477_232541478del GRCh38
NC_000002.11:g.233406187_233406188del , CM000664.1:g.233406187_233406188del GRCh37
NC_000002.10:g.233114431_233114432del NCBI36
NG_012954.1:g.6751_6752del
NG_012954.2:g.6786_6787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.454_455del MANE Select ENSP00000498757.1:p.Ile152LeufsTer25
ENST00000389492.3:c.350+766_350+767del ENSP00000374143.3:n.350+766_350+767del
ENST00000389494.7:c.454_455del ENSP00000374145.3:p.Ile152LeufsTer25
ENST00000485094.1:n.475_476del
NM_005199.4:c.454_455del NP_005190.4:p.Ile152LeufsTer25
NM_005199.5:c.454_455del MANE Select NP_005190.4:p.Ile152LeufsTer25
Search 100 bp 5'
Search 100 bp 3'