Canonical Allele Identifier: CA2754656892

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541610_232541611insCAGAAGCC , CM000664.2:g.232541610_232541611insCAGAAGCC	GRCh38
NC_000002.11:g.233406320_233406321insCAGAAGCC , CM000664.1:g.233406320_233406321insCAGAAGCC	GRCh37
NC_000002.10:g.233114564_233114565insCAGAAGCC	NCBI36
NG_012954.1:g.6884_6885insCAGAAGCC
NG_012954.2:g.6919_6920insCAGAAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+81_506+82insCAGAAGCC MANE Select	ENSP00000498757.1:n.506+81_506+82insCAGAAGCC
ENST00000389492.3:c.351-813_351-812insCAGAAGCC	ENSP00000374143.3:n.351-813_351-812insCAGAAGCC
ENST00000389494.7:c.506+81_506+82insCAGAAGCC	ENSP00000374145.3:n.506+81_506+82insCAGAAGCC
ENST00000485094.1:n.608_609insCAGAAGCC
NM_005199.4:c.506+81_506+82insCAGAAGCC	NP_005190.4:n.506+81_506+82insCAGAAGCC
NM_005199.5:c.506+81_506+82insCAGAAGCC MANE Select	NP_005190.4:n.506+81_506+82insCAGAAGCC