Canonical Allele Identifier: CA2571119591

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719761_74719768del , CM000677.2:g.74719761_74719768del	GRCh38
NC_000015.9:g.75012102_75012109del , CM000677.1:g.75012102_75012109del	GRCh37
NC_000015.8:g.72799155_72799162del	NCBI36
NG_008431.1:g.2220_2227del
NG_008431.2:g.2220_2227del
NG_061374.1:g.10761_10768del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*721_*728del MANE Select	ENSP00000369050.3:n.*721_*728del
ENST00000379727.7:c.*721_*728del	ENSP00000369050.3:n.*721_*728del
ENST00000395048.6:c.*721_*728del	ENSP00000378488.2:n.*721_*728del
ENST00000612821.4:c.2176_2183del	ENSP00000479744.1:n.2176_2183del
ENST00000617691.4:c.*721_*728del	ENSP00000482863.1:n.*721_*728del
NM_000499.3:c.*721_*728del	NP_000490.1:n.*721_*728del
XM_005254185.1:c.*721_*728del	XP_005254242.1:n.*721_*728del
NM_000499.5:c.*721_*728del	NP_000490.1:n.*721_*728del
NM_001319216.2:c.*721_*728del	NP_001306145.1:n.*721_*728del
NM_001319217.2:c.*721_*728del MANE Select	NP_001306146.1:n.*721_*728del