Canonical Allele Identifier: CA2840394685

Gene: CYP1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74751924dup , CM000677.2:g.74751924dup	GRCh38
NC_000015.9:g.75044265dup , CM000677.1:g.75044265dup	GRCh37
NC_000015.8:g.72831318dup	NCBI36
NG_008431.1:g.34383dup
NG_008431.2:g.34383dup
NG_061543.1:g.8080dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1042+70dup MANE Select	ENSP00000342007.4:n.1042+70dup
ENST00000343932.4:c.1042+70dup	ENSP00000342007.4:n.1042+70dup
NM_000761.4:c.1042+70dup	NP_000752.2:n.1042+70dup
NM_000761.5:c.1042+70dup MANE Select	NP_000752.2:n.1042+70dup