Canonical Allele Identifier: CA2187827039
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754805_74754806delinsAC , CM000677.2:g.74754805_74754806delinsAC GRCh38
NC_000015.9:g.75047146_75047147delinsAC , CM000677.1:g.75047146_75047147delinsAC GRCh37
NC_000015.8:g.72834199_72834200delinsAC NCBI36
NG_008431.1:g.37264_37265delinsAC
NG_008431.2:g.37264_37265delinsAC
NG_061543.1:g.10961_10962delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1268_1269delinsAC MANE Select ENSP00000342007.4:p.Asp423=
ENST00000343932.4:c.1268_1269delinsAC ENSP00000342007.4:p.Asp423=
NM_000761.4:c.1268_1269delinsAC NP_000752.2:p.Asp423=
NM_000761.5:c.1268_1269delinsAC MANE Select NP_000752.2:p.Asp423=