Canonical Allele Identifier: CA2804765441

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719559_74719560del , CM000677.2:g.74719559_74719560del	GRCh38
NC_000015.9:g.75011900_75011901del , CM000677.1:g.75011900_75011901del	GRCh37
NC_000015.8:g.72798953_72798954del	NCBI36
NG_008431.1:g.2018_2019del
NG_008431.2:g.2018_2019del
NG_061374.1:g.10971_10972del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*931_*932del MANE Select	ENSP00000369050.3:n.*931_*932del
ENST00000379727.7:c.*931_*932del	ENSP00000369050.3:n.*931_*932del
ENST00000395048.6:c.*931_*932del	ENSP00000378488.2:n.*931_*932del
ENST00000612821.4:c.2386_2387del	ENSP00000479744.1:n.2386_2387del
ENST00000617691.4:c.*931_*932del	ENSP00000482863.1:n.*931_*932del
NM_000499.3:c.*931_*932del	NP_000490.1:n.*931_*932del
XM_005254185.1:c.*931_*932del	XP_005254242.1:n.*931_*932del
NM_000499.5:c.*931_*932del	NP_000490.1:n.*931_*932del
NM_001319216.2:c.*931_*932del	NP_001306145.1:n.*931_*932del
NM_001319217.2:c.*931_*932del MANE Select	NP_001306146.1:n.*931_*932del