Canonical Allele Identifier: CA10264745

Gene: CYP2D6

Linked Data

• dbSNP Id: rs550835698
• ExAC: 22:42523832 A / AGAT
• gnomAD v2: 22-42523832-A-AGAT
• gnomAD v3: 22-42127830-A-AGAT
• gnomAD v4: 22-42127830-A-AGAT
• MyVariant Identifiers: chr22:g.42523832_42523833insGAT (hg19) ; chr22:g.42127830_42127831insGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127832_42127834dup , CM000684.2:g.42127832_42127834dup	GRCh38
NC_000022.10:g.42523834_42523836dup , CM000684.1:g.42523834_42523836dup	GRCh37
NC_000022.9:g.40853778_40853780dup	NCBI36
NG_008376.3:g.7159_7161dup
NG_008376.4:g.7978_7980dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+9_783+11dup	ENSP00000353241.6:n.783+9_783+11dup
ENST00000645361.2:c.985+9_985+11dup MANE Select	ENSP00000496150.1:n.985+9_985+11dup
ENST00000359033.4:c.832+9_832+11dup	ENSP00000351927.4:n.832+9_832+11dup
ENST00000360124.9:c.603+9_603+11dup	ENSP00000353241.5:n.603+9_603+11dup
ENST00000360608.9:c.985+9_985+11dup	ENSP00000353820.5:n.985+9_985+11dup
ENST00000389970.7:c.919+9_919+11dup	ENSP00000374620.4:n.919+9_919+11dup
ENST00000488442.1:n.1709+9_1709+11dup
NM_000106.5:c.985+9_985+11dup	NP_000097.3:n.985+9_985+11dup
NM_001025161.2:c.832+9_832+11dup	NP_001020332.2:n.832+9_832+11dup
XM_011529966.1:c.985+9_985+11dup	XP_011528268.1:n.985+9_985+11dup
XM_011529967.1:c.985+9_985+11dup	XP_011528269.1:n.985+9_985+11dup
XM_011529968.1:c.985+9_985+11dup	XP_011528270.1:n.985+9_985+11dup
XM_011529969.1:c.841+9_841+11dup	XP_011528271.1:n.841+9_841+11dup
XM_011529970.1:c.832+9_832+11dup	XP_011528272.1:n.832+9_832+11dup
XM_011529971.1:c.841+9_841+11dup	XP_011528273.1:n.841+9_841+11dup
XM_011529972.1:c.844-199_844-197dup	XP_011528274.1:n.844-199_844-197dup
NM_000106.6:c.985+9_985+11dup MANE Select	NP_000097.3:n.985+9_985+11dup
NM_001025161.3:c.832+9_832+11dup	NP_001020332.2:n.832+9_832+11dup