Canonical Allele Identifier: CA2187825667
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752057_74752059delinsAAG , CM000677.2:g.74752057_74752059delinsAAG GRCh38
NC_000015.9:g.75044398_75044400delinsAAG , CM000677.1:g.75044398_75044400delinsAAG GRCh37
NC_000015.8:g.72831451_72831453delinsAAG NCBI36
NG_008431.1:g.34516_34518delinsAAG
NG_008431.2:g.34516_34518delinsAAG
NG_061543.1:g.8213_8215delinsAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-67_1043-65delinsAAG MANE Select ENSP00000342007.4:n.1043-67_1043-65delins...
ENST00000343932.4:c.1043-67_1043-65delinsAAG ENSP00000342007.4:n.1043-67_1043-65delins...
NM_000761.4:c.1043-67_1043-65delinsAAG NP_000752.2:n.1043-67_1043-65delinsAAG
NM_000761.5:c.1043-67_1043-65delinsAAG MANE Select NP_000752.2:n.1043-67_1043-65delinsAAG