Canonical Allele Identifier: CA2187814521

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719673_74719697delinsATGCAGGCTAGAATAGAAGGATTGT , CM000677.2:g.74719673_74719697delinsATGCAGGCTAGAATAGAAGGATTGT	GRCh38
NC_000015.9:g.75012014_75012038delinsATGCAGGCTAGAATAGAAGGATTGT , CM000677.1:g.75012014_75012038delinsATGCAGGCTAGAATAGAAGGATTGT	GRCh37
NC_000015.8:g.72799067_72799091delinsATGCAGGCTAGAATAGAAGGATTGT	NCBI36
NG_008431.1:g.2132_2156delinsATGCAGGCTAGAATAGAAGGATTGT
NG_008431.2:g.2132_2156delinsATGCAGGCTAGAATAGAAGGATTGT
NG_061374.1:g.10832_10856delinsACAATCCTTCTATTCTAGCCTGCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT MANE Select	ENSP00000369050.3:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
ENST00000379727.7:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	ENSP00000369050.3:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
ENST00000395048.6:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	ENSP00000378488.2:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
ENST00000612821.4:c.2247_2271delinsACAATCCTTCTATTCTAGCCTGCAT	ENSP00000479744.1:n.2247_2271delinsACAATCCTTCTATTCTAGCCTGCAT
ENST00000617691.4:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	ENSP00000482863.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
NM_000499.3:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	NP_000490.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
XM_005254185.1:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	XP_005254242.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
NM_000499.5:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	NP_000490.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
NM_001319216.2:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT	NP_001306145.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT
NM_001319217.2:c.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT MANE Select	NP_001306146.1:n.*792_*816delinsACAATCCTTCTATTCTAGCCTGCAT