Canonical Allele Identifier: CA2187816818
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs2063202068

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74724762_74724764del , CM000677.2:g.74724762_74724764del GRCh38
NC_000015.9:g.75017103_75017105del , CM000677.1:g.75017103_75017105del GRCh37
NC_000015.8:g.72804156_72804158del NCBI36
NG_008431.1:g.7221_7223del
NG_008431.2:g.7221_7223del
NG_061374.1:g.5768_5770del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.-30+680_-30+682del MANE Select ENSP00000369050.3:n.-30+680_-30+682del
ENST00000379727.7:c.-30+680_-30+682del ENSP00000369050.3:n.-30+680_-30+682del
ENST00000395048.6:c.-27+680_-27+682del ENSP00000378488.2:n.-27+680_-27+682del
ENST00000395049.8:c.-30+680_-30+682del ENSP00000378489.4:n.-30+680_-30+682del
ENST00000562201.5:c.-27+680_-27+682del ENSP00000455340.1:n.-27+680_-27+682del
ENST00000564596.5:c.-221+680_-221+682del ENSP00000457668.1:n.-221+680_-221+682del
ENST00000566503.1:c.-221+680_-221+682del ENSP00000455846.1:n.-221+680_-221+682del
ENST00000567032.5:c.-30+404_-30+406del ENSP00000456585.1:n.-30+404_-30+406del
ENST00000569630.5:c.-27+680_-27+682del ENSP00000455051.1:n.-27+680_-27+682del
ENST00000617691.4:c.-27+680_-27+682del ENSP00000482863.1:n.-27+680_-27+682del
NM_000499.3:c.-27+680_-27+682del NP_000490.1:n.-27+680_-27+682del
XM_005254185.1:c.-30+680_-30+682del XP_005254242.1:n.-30+680_-30+682del
NM_000499.5:c.-27+680_-27+682del NP_000490.1:n.-27+680_-27+682del
NM_001319216.2:c.-30+680_-30+682del NP_001306145.1:n.-30+680_-30+682del
NM_001319217.2:c.-30+680_-30+682del MANE Select NP_001306146.1:n.-30+680_-30+682del