Canonical Allele Identifier: CA639827887

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1258138204
• gnomAD v2: 22-42522758-T-TGGGGA
• gnomAD v3: 22-42126756-T-TGGGGA
• gnomAD v4: 22-42126756-T-TGGGGA
• MyVariant Identifiers: chr22:g.42522763_42522764insGGGGA (hg19) ; chr22:g.42522758_42522759insGGGGA (hg19) ; chr22:g.42126756_42126757insGGGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126766_42126770dup , CM000684.2:g.42126766_42126770dup	GRCh38
NC_000022.10:g.42522768_42522772dup , CM000684.1:g.42522768_42522772dup	GRCh37
NC_000022.9:g.40852712_40852716dup	NCBI36
NG_008376.3:g.8231_8235dup
NG_008376.4:g.9050_9054dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1114-9_1114-5dup	ENSP00000353241.6:n.1114-9_1114-5dup
ENST00000645361.2:c.1316-9_1316-5dup MANE Select	ENSP00000496150.1:n.1316-9_1316-5dup
ENST00000359033.4:c.1163-9_1163-5dup	ENSP00000351927.4:n.1163-9_1163-5dup
ENST00000360124.9:c.934-9_934-5dup	ENSP00000353241.5:n.934-9_934-5dup
ENST00000360608.9:c.1316-9_1316-5dup	ENSP00000353820.5:n.1316-9_1316-5dup
ENST00000389970.7:c.1307-9_1307-5dup	ENSP00000374620.4:n.1307-9_1307-5dup
ENST00000488442.1:n.2040-9_2040-5dup
NM_000106.5:c.1316-9_1316-5dup	NP_000097.3:n.1316-9_1316-5dup
NM_001025161.2:c.1163-9_1163-5dup	NP_001020332.2:n.1163-9_1163-5dup
XM_011529966.1:c.1316-9_1316-5dup	XP_011528268.1:n.1316-9_1316-5dup
XM_011529967.1:c.1316-9_1316-5dup	XP_011528269.1:n.1316-9_1316-5dup
XM_011529968.1:c.1316-9_1316-5dup	XP_011528270.1:n.1316-9_1316-5dup
XM_011529969.1:c.1172-9_1172-5dup	XP_011528271.1:n.1172-9_1172-5dup
XM_011529970.1:c.1163-9_1163-5dup	XP_011528272.1:n.1163-9_1163-5dup
XM_011529971.1:c.1172-9_1172-5dup	XP_011528273.1:n.1172-9_1172-5dup
NM_000106.6:c.1316-9_1316-5dup MANE Select	NP_000097.3:n.1316-9_1316-5dup
NM_001025161.3:c.1163-9_1163-5dup	NP_001020332.2:n.1163-9_1163-5dup