Canonical Allele Identifier: CA2629509385
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751922_74751923insTCC , CM000677.2:g.74751922_74751923insTCC GRCh38
NC_000015.9:g.75044263_75044264insTCC , CM000677.1:g.75044263_75044264insTCC GRCh37
NC_000015.8:g.72831316_72831317insTCC NCBI36
NG_008431.1:g.34381_34382insTCC
NG_008431.2:g.34381_34382insTCC
NG_061543.1:g.8078_8079insTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+68_1042+69insTCC MANE Select ENSP00000342007.4:n.1042+68_1042+69insTCC...
ENST00000343932.4:c.1042+68_1042+69insTCC ENSP00000342007.4:n.1042+68_1042+69insTCC...
NM_000761.4:c.1042+68_1042+69insTCC NP_000752.2:n.1042+68_1042+69insTCC
NM_000761.5:c.1042+68_1042+69insTCC MANE Select NP_000752.2:n.1042+68_1042+69insTCC