Canonical Allele Identifier: CA2187824204
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74748899_74748900delinsTA , CM000677.2:g.74748899_74748900delinsTA GRCh38
NC_000015.9:g.75041240_75041241delinsTA , CM000677.1:g.75041240_75041241delinsTA GRCh37
NC_000015.8:g.72828293_72828294delinsTA NCBI36
NG_008431.1:g.31358_31359delinsTA
NG_008431.2:g.31358_31359delinsTA
NG_061543.1:g.5055_5056delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+2_-10+3delinsTA MANE Select ENSP00000342007.4:n.-10+2_-10+3delinsTA
ENST00000343932.4:c.-10+2_-10+3delinsTA ENSP00000342007.4:n.-10+2_-10+3delinsTA
NM_000761.4:c.-10+2_-10+3delinsTA NP_000752.2:n.-10+2_-10+3delinsTA
NM_000761.5:c.-10+2_-10+3delinsTA MANE Select NP_000752.2:n.-10+2_-10+3delinsTA