Canonical Allele Identifier: CA10264740

Gene: CYP2D6

Linked Data

• dbSNP Id: rs746736981
• ExAC: 22:42523822 ACT / A
• gnomAD v2: 22-42523822-ACT-A
• gnomAD v4: 22-42127820-ACT-A
• MyVariant Identifiers: chr22:g.42523823_42523824del (hg19) ; chr22:g.42127821_42127822del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127821_42127822del , CM000684.2:g.42127821_42127822del	GRCh38
NC_000022.10:g.42523823_42523824del , CM000684.1:g.42523823_42523824del	GRCh37
NC_000022.9:g.40853767_40853768del	NCBI36
NG_008376.3:g.7170_7171del
NG_008376.4:g.7989_7990del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.783+20_783+21del	ENSP00000353241.6:n.783+20_783+21del
ENST00000645361.2:c.985+20_985+21del MANE Select	ENSP00000496150.1:n.985+20_985+21del
ENST00000359033.4:c.832+20_832+21del	ENSP00000351927.4:n.832+20_832+21del
ENST00000360124.9:c.603+20_603+21del	ENSP00000353241.5:n.603+20_603+21del
ENST00000360608.9:c.985+20_985+21del	ENSP00000353820.5:n.985+20_985+21del
ENST00000389970.7:c.920-13_920-12del	ENSP00000374620.4:n.920-13_920-12del
ENST00000488442.1:n.1709+20_1709+21del
NM_000106.5:c.985+20_985+21del	NP_000097.3:n.985+20_985+21del
NM_001025161.2:c.832+20_832+21del	NP_001020332.2:n.832+20_832+21del
XM_011529966.1:c.985+20_985+21del	XP_011528268.1:n.985+20_985+21del
XM_011529967.1:c.985+20_985+21del	XP_011528269.1:n.985+20_985+21del
XM_011529968.1:c.985+20_985+21del	XP_011528270.1:n.985+20_985+21del
XM_011529969.1:c.841+20_841+21del	XP_011528271.1:n.841+20_841+21del
XM_011529970.1:c.832+20_832+21del	XP_011528272.1:n.832+20_832+21del
XM_011529971.1:c.841+20_841+21del	XP_011528273.1:n.841+20_841+21del
XM_011529972.1:c.844-188_844-187del	XP_011528274.1:n.844-188_844-187del
NM_000106.6:c.985+20_985+21del MANE Select	NP_000097.3:n.985+20_985+21del
NM_001025161.3:c.832+20_832+21del	NP_001020332.2:n.832+20_832+21del