Canonical Allele Identifier: CA2187825750
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752214_74752217delinsACTC , CM000677.2:g.74752214_74752217delinsACTC GRCh38
NC_000015.9:g.75044555_75044558delinsACTC , CM000677.1:g.75044555_75044558delinsACTC GRCh37
NC_000015.8:g.72831608_72831611delinsACTC NCBI36
NG_008431.1:g.34673_34676delinsACTC
NG_008431.2:g.34673_34676delinsACTC
NG_061543.1:g.8370_8373delinsACTC

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1133_1136delinsACTC MANE Select ENSP00000342007.4:p.His378=
ENST00000343932.4:c.1133_1136delinsACTC ENSP00000342007.4:p.His378=
NM_000761.4:c.1133_1136delinsACTC NP_000752.2:p.His378=
NM_000761.5:c.1133_1136delinsACTC MANE Select NP_000752.2:p.His378=