Canonical Allele Identifier: CA2629509376
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751919_74751920insGA , CM000677.2:g.74751919_74751920insGA GRCh38
NC_000015.9:g.75044260_75044261insGA , CM000677.1:g.75044260_75044261insGA GRCh37
NC_000015.8:g.72831313_72831314insGA NCBI36
NG_008431.1:g.34378_34379insGA
NG_008431.2:g.34378_34379insGA
NG_061543.1:g.8075_8076insGA

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+65_1042+66insGA MANE Select ENSP00000342007.4:n.1042+65_1042+66insGA
ENST00000343932.4:c.1042+65_1042+66insGA ENSP00000342007.4:n.1042+65_1042+66insGA
NM_000761.4:c.1042+65_1042+66insGA NP_000752.2:n.1042+65_1042+66insGA
NM_000761.5:c.1042+65_1042+66insGA MANE Select NP_000752.2:n.1042+65_1042+66insGA