Canonical Allele Identifier: CA2187826944

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754601_74754603delinsCAA , CM000677.2:g.74754601_74754603delinsCAA	GRCh38
NC_000015.9:g.75046942_75046944delinsCAA , CM000677.1:g.75046942_75046944delinsCAA	GRCh37
NC_000015.8:g.72833995_72833997delinsCAA	NCBI36
NG_008431.1:g.37060_37062delinsCAA
NG_008431.2:g.37060_37062delinsCAA
NG_061543.1:g.10757_10759delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1254-190_1254-188delinsCAA MANE Select	ENSP00000342007.4:n.1254-190_1254-188delinsCAA
ENST00000343932.4:c.1254-190_1254-188delinsCAA	ENSP00000342007.4:n.1254-190_1254-188delinsCAA
NM_000761.4:c.1254-190_1254-188delinsCAA	NP_000752.2:n.1254-190_1254-188delinsCAA
NM_000761.5:c.1254-190_1254-188delinsCAA MANE Select	NP_000752.2:n.1254-190_1254-188delinsCAA