Canonical Allele Identifier: CA2663621473
Gene: CHRNG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232539888dup , CM000664.2:g.232539888dup GRCh38
NC_000002.11:g.233404598dup , CM000664.1:g.233404598dup GRCh37
NC_000002.10:g.233112842dup NCBI36
NG_012954.1:g.5162dup
NG_012954.2:g.5197dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000651502.1:c.55+86dup MANE Select ENSP00000498757.1:n.55+86dup
ENST00000389492.3:c.55+86dup ENSP00000374143.3:n.55+86dup
ENST00000389494.7:c.55+86dup ENSP00000374145.3:n.55+86dup
ENST00000485094.1:n.76+86dup
NM_005199.4:c.55+86dup NP_005190.4:n.55+86dup
NM_005199.5:c.55+86dup MANE Select NP_005190.4:n.55+86dup