Canonical Allele Identifier: CA2577737215

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128928_42128929insAAAG , CM000684.2:g.42128928_42128929insAAAG	GRCh38
NC_000022.10:g.42524930_42524931insAAAG , CM000684.1:g.42524930_42524931insAAAG	GRCh37
NC_000022.9:g.40854874_40854875insAAAG	NCBI36
NG_008376.3:g.6064_6065insTTTC
NG_008376.4:g.6883_6884insTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.369_370insTTTC	ENSP00000353241.6:p.Asn124PhefsTer?
ENST00000645361.2:c.522_523insTTTC MANE Select	ENSP00000496150.1:p.Asn175PhefsTer?
ENST00000359033.4:c.369_370insTTTC	ENSP00000351927.4:p.Asn124PhefsTer?
ENST00000360124.9:c.189_190insTTTC	ENSP00000353241.5:p.Asn64PhefsTer?
ENST00000360608.9:c.522_523insTTTC	ENSP00000353820.5:p.Asn175PhefsTer?
ENST00000389970.7:c.456_457insTTTC	ENSP00000374620.4:p.Asn153PhefsTer?
ENST00000488442.1:n.1246_1247insTTTC
NM_000106.5:c.522_523insTTTC	NP_000097.3:p.Asn175PhefsTer?
NM_001025161.2:c.369_370insTTTC	NP_001020332.2:p.Asn124PhefsTer?
XM_011529966.1:c.522_523insTTTC	XP_011528268.1:p.Asn175PhefsTer?
XM_011529967.1:c.522_523insTTTC	XP_011528269.1:p.Asn175PhefsTer?
XM_011529968.1:c.522_523insTTTC	XP_011528270.1:p.Asn175PhefsTer?
XM_011529969.1:c.378_379insTTTC	XP_011528271.1:p.Asn127PhefsTer?
XM_011529970.1:c.369_370insTTTC	XP_011528272.1:p.Asn124PhefsTer?
XM_011529971.1:c.378_379insTTTC	XP_011528273.1:p.Asn127PhefsTer?
XM_011529972.1:c.522_523insTTTC	XP_011528274.1:p.Asn175PhefsTer?
NM_000106.6:c.522_523insTTTC MANE Select	NP_000097.3:p.Asn175PhefsTer?
NM_001025161.3:c.369_370insTTTC	NP_001020332.2:p.Asn124PhefsTer?