Canonical Allele Identifier: CA2187827320
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755365_74755366delinsAC , CM000677.2:g.74755365_74755366delinsAC GRCh38
NC_000015.9:g.75047706_75047707delinsAC , CM000677.1:g.75047706_75047707delinsAC GRCh37
NC_000015.8:g.72834759_72834760delinsAC NCBI36
NG_008431.1:g.37824_37825delinsAC
NG_008431.2:g.37824_37825delinsAC
NG_061543.1:g.11521_11522delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*277_*278delinsAC MANE Select ENSP00000342007.4:n.*277_*278delinsAC
ENST00000343932.4:c.*277_*278delinsAC ENSP00000342007.4:n.*277_*278delinsAC
NM_000761.4:c.*277_*278delinsAC NP_000752.2:n.*277_*278delinsAC
NM_000761.5:c.*277_*278delinsAC MANE Select NP_000752.2:n.*277_*278delinsAC