Canonical Allele Identifier: CA1335316820

Gene: CHRNG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.232541595_232541638delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG , CM000664.2:g.232541595_232541638delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	GRCh38
NC_000002.11:g.233406305_233406348delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG , CM000664.1:g.233406305_233406348delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	GRCh37
NC_000002.10:g.233114549_233114592delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	NCBI36
NG_012954.1:g.6869_6912delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG
NG_012954.2:g.6904_6947delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651502.1:c.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG MANE Select	ENSP00000498757.1:n.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTG...
ENST00000389492.3:c.351-828_351-785delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	ENSP00000374143.3:n.351-828_351-785delinsAAGGCCTGGGCAAGGCTTCT...
ENST00000389494.7:c.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	ENSP00000374145.3:n.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTG...
ENST00000485094.1:n.593_636delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG
NM_005199.4:c.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG	NP_005190.4:n.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTG...
NM_005199.5:c.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTGGCTCTGGCAGCACCTAG MANE Select	NP_005190.4:n.506+66_506+109delinsAAGGCCTGGGCAAGGCTTCTGGCCTTG...