Canonical Allele Identifier: CA639827936

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1210289938
• gnomAD v2: 22-42524137-CCCA-C
• gnomAD v4: 22-42128135-CCCA-C
• MyVariant Identifiers: chr22:g.42524138_42524140del (hg19) ; chr22:g.42128136_42128138del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128141_42128143del , CM000684.2:g.42128141_42128143del	GRCh38
NC_000022.10:g.42524143_42524145del , CM000684.1:g.42524143_42524145del	GRCh37
NC_000022.9:g.40854087_40854089del	NCBI36
NG_008376.3:g.6854_6856del
NG_008376.4:g.7673_7675del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.690+36_690+38del	ENSP00000353241.6:n.690+36_690+38del
ENST00000645361.2:c.843+36_843+38del MANE Select	ENSP00000496150.1:n.843+36_843+38del
ENST00000359033.4:c.690+36_690+38del	ENSP00000351927.4:n.690+36_690+38del
ENST00000360124.9:c.510+36_510+38del	ENSP00000353241.5:n.510+36_510+38del
ENST00000360608.9:c.843+36_843+38del	ENSP00000353820.5:n.843+36_843+38del
ENST00000389970.7:c.777+36_777+38del	ENSP00000374620.4:n.777+36_777+38del
ENST00000488442.1:n.1567+36_1567+38del
NM_000106.5:c.843+36_843+38del	NP_000097.3:n.843+36_843+38del
NM_001025161.2:c.690+36_690+38del	NP_001020332.2:n.690+36_690+38del
XM_011529966.1:c.843+36_843+38del	XP_011528268.1:n.843+36_843+38del
XM_011529967.1:c.843+36_843+38del	XP_011528269.1:n.843+36_843+38del
XM_011529968.1:c.843+36_843+38del	XP_011528270.1:n.843+36_843+38del
XM_011529969.1:c.699+36_699+38del	XP_011528271.1:n.699+36_699+38del
XM_011529970.1:c.690+36_690+38del	XP_011528272.1:n.690+36_690+38del
XM_011529971.1:c.699+36_699+38del	XP_011528273.1:n.699+36_699+38del
XM_011529972.1:c.843+36_843+38del	XP_011528274.1:n.843+36_843+38del
NM_000106.6:c.843+36_843+38del MANE Select	NP_000097.3:n.843+36_843+38del
NM_001025161.3:c.690+36_690+38del	NP_001020332.2:n.690+36_690+38del