Canonical Allele Identifier: CA2663621445
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539861_232539862insA , CM000664.2:g.232539861_232539862insA GRCh38
NC_000002.11:g.233404571_233404572insA , CM000664.1:g.233404571_233404572insA GRCh37
NC_000002.10:g.233112815_233112816insA NCBI36
NG_012954.1:g.5135_5136insA
NG_012954.2:g.5170_5171insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.55+59_55+60insA MANE Select ENSP00000498757.1:n.55+59_55+60insA
ENST00000389492.3:c.55+59_55+60insA ENSP00000374143.3:n.55+59_55+60insA
ENST00000389494.7:c.55+59_55+60insA ENSP00000374145.3:n.55+59_55+60insA
ENST00000485094.1:n.76+59_76+60insA
NM_005199.4:c.55+59_55+60insA NP_005190.4:n.55+59_55+60insA
NM_005199.5:c.55+59_55+60insA MANE Select NP_005190.4:n.55+59_55+60insA