Canonical Allele Identifier: CA411778123

Gene: CYP2D7

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42141217C>A , CM000684.2:g.42141217C>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435101.2:n.231G>T
ENST00000651010.1:n.3084G>T
ENST00000358097.8:c.1109G>T	ENSP00000445124.1:p.Arg370Leu
ENST00000433992.2:c.1166G>T	ENSP00000439604.1:p.Arg389Leu
ENST00000435101.1:c.231G>T	ENSP00000437680.2:n.231G>T
ENST00000612115.1:c.1162G>T	ENSP00000484065.1:p.Val388Phe
ENST00000614967.4:c.955G>T	ENSP00000481168.1:p.Val319Phe
NR_002570.3:n.1220G>T
NM_001348386.2:c.1165G>T	NP_001335315.1:p.Val389Phe
NR_002570.5:n.1128G>T
NR_145674.2:n.1185G>T
NM_001348386.3:c.1165G>T	NP_001335315.1:p.Val389Phe
NR_002570.6:n.1128G>T
NR_145674.3:n.1185G>T