Canonical Allele Identifier: CA2406586634

Gene: CYP2D7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42142339_42142341delinsGCC , CM000684.2:g.42142339_42142341delinsGCC	GRCh38
NC_000022.10:g.42538349_42538351delinsGCC , CM000684.1:g.42538349_42538351delinsGCC	GRCh37
NC_000022.9:g.40868293_40868295delinsGCC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000651010.1:n.2620+138_2620+140delinsGGC
ENST00000358097.8:c.667+138_667+140delinsGGC	ENSP00000445124.1:n.667+138_667+140delinsGGC
ENST00000433992.2:c.667+138_667+140delinsGGC	ENSP00000439604.1:n.667+138_667+140delinsGGC
ENST00000610593.4:n.752+138_752+140delinsGGC
ENST00000612115.1:c.666+138_666+140delinsGGC	ENSP00000484065.1:n.666+138_666+140delinsGGC
ENST00000614967.4:c.513+138_513+140delinsGGC	ENSP00000481168.1:n.513+138_513+140delinsGGC
NR_002570.3:n.778+138_778+140delinsGGC
NM_001348386.2:c.666+138_666+140delinsGGC	NP_001335315.1:n.666+138_666+140delinsGGC
NR_002570.5:n.686+138_686+140delinsGGC
NR_145674.2:n.686+138_686+140delinsGGC
NM_001348386.3:c.666+138_666+140delinsGGC	NP_001335315.1:n.666+138_666+140delinsGGC
NR_002570.6:n.686+138_686+140delinsGGC
NR_145674.3:n.686+138_686+140delinsGGC