Canonical Allele Identifier: CA645577949
Gene: CYP1A2 HGNC NCBI

Linked Data

COSMIC: COSM290942
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749947_74749948delinsCC , CM000677.2:g.74749947_74749948delinsCC GRCh38
NC_000015.9:g.75042288_75042289delinsCC , CM000677.1:g.75042288_75042289delinsCC GRCh37
NC_000015.8:g.72829341_72829342delinsCC NCBI36
NG_008431.1:g.32406_32407delinsCC
NG_008431.2:g.32406_32407delinsCC
NG_061543.1:g.6103_6104delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.209_210delinsCC MANE Select ENSP00000342007.4:p.Gln70Pro
ENST00000343932.4:c.209_210delinsCC ENSP00000342007.4:p.Gln70Pro
NM_000761.4:c.209_210delinsCC NP_000752.2:p.Gln70Pro
NM_000761.5:c.209_210delinsCC MANE Select NP_000752.2:p.Gln70Pro
Search 100 bp 5'
Search 100 bp 3'