Canonical Allele Identifier: CA2406586637

Gene: CYP2D7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142341_42142344delinsCCTT , CM000684.2:g.42142341_42142344delinsCCTT	GRCh38
NC_000022.10:g.42538351_42538354delinsCCTT , CM000684.1:g.42538351_42538354delinsCCTT	GRCh37
NC_000022.9:g.40868295_40868298delinsCCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651010.1:n.2620+135_2620+138delinsAAGG
ENST00000358097.8:c.667+135_667+138delinsAAGG	ENSP00000445124.1:n.667+135_667+138delinsAAGG
ENST00000433992.2:c.667+135_667+138delinsAAGG	ENSP00000439604.1:n.667+135_667+138delinsAAGG
ENST00000610593.4:n.752+135_752+138delinsAAGG
ENST00000612115.1:c.666+135_666+138delinsAAGG	ENSP00000484065.1:n.666+135_666+138delinsAAGG
ENST00000614967.4:c.513+135_513+138delinsAAGG	ENSP00000481168.1:n.513+135_513+138delinsAAGG
NR_002570.3:n.778+135_778+138delinsAAGG
NM_001348386.2:c.666+135_666+138delinsAAGG	NP_001335315.1:n.666+135_666+138delinsAAGG
NR_002570.5:n.686+135_686+138delinsAAGG
NR_145674.2:n.686+135_686+138delinsAAGG
NM_001348386.3:c.666+135_666+138delinsAAGG	NP_001335315.1:n.666+135_666+138delinsAAGG
NR_002570.6:n.686+135_686+138delinsAAGG
NR_145674.3:n.686+135_686+138delinsAAGG