Canonical Allele Identifier: CA472262071

Gene: CYP2E1

Linked Data

• MyVariant Identifiers: chr10:g.135352309C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133538805C>A , CM000672.2:g.133538805C>A	GRCh38
NC_000010.10:g.135352309C>A , CM000672.1:g.135352309C>A	GRCh37
NC_000010.9:g.135202299C>A	NCBI36
NG_008383.1:g.16443C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252945.8:c.1323C>A MANE Select	ENSP00000252945.3:p.Gly441=
ENST00000252945.7:c.1323C>A	ENSP00000252945.3:p.Gly441=
ENST00000368520.1:n.1358+913C>A
ENST00000418356.1:c.912C>A	ENSP00000397299.1:p.Gly304=
ENST00000421586.5:c.1062C>A	ENSP00000412754.1:p.Gly354=
ENST00000463117.6:c.1323C>A	ENSP00000440689.1:p.Gly441=
ENST00000469258.1:n.419C>A
ENST00000541080.5:c.739C>A
NM_000773.3:c.1323C>A	NP_000764.1:p.Gly441=
NM_000773.4:c.1323C>A MANE Select	NP_000764.1:p.Gly441=