Canonical Allele Identifier: CA2731198294

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2141742579

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755364_74755365insC , CM000677.2:g.74755364_74755365insC	GRCh38
NC_000015.9:g.75047705_75047706insC , CM000677.1:g.75047705_75047706insC	GRCh37
NC_000015.8:g.72834758_72834759insC	NCBI36
NG_008431.1:g.37823_37824insC
NG_008431.2:g.37823_37824insC
NG_061543.1:g.11520_11521insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*276_*277insC MANE Select	ENSP00000342007.4:n.*276_*277insC
ENST00000343932.4:c.*276_*277insC	ENSP00000342007.4:n.*276_*277insC
NM_000761.4:c.*276_*277insC	NP_000752.2:n.*276_*277insC
NM_000761.5:c.*276_*277insC MANE Select	NP_000752.2:n.*276_*277insC