Canonical Allele Identifier: CA2657033765

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42128894-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128895_42128897del , CM000684.2:g.42128895_42128897del	GRCh38
NC_000022.10:g.42524897_42524899del , CM000684.1:g.42524897_42524899del	GRCh37
NC_000022.9:g.40854841_40854843del	NCBI36
NG_008376.3:g.6095_6097del
NG_008376.4:g.6914_6916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.400_402del	ENSP00000353241.6:p.Val134del
ENST00000645361.2:c.553_555del MANE Select	ENSP00000496150.1:p.Val185del
ENST00000359033.4:c.400_402del	ENSP00000351927.4:p.Val134del
ENST00000360124.9:c.220_222del	ENSP00000353241.5:p.Val74del
ENST00000360608.9:c.553_555del	ENSP00000353820.5:p.Val185del
ENST00000389970.7:c.487_489del	ENSP00000374620.4:p.Val163del
ENST00000488442.1:n.1277_1279del
NM_000106.5:c.553_555del	NP_000097.3:p.Val185del
NM_001025161.2:c.400_402del	NP_001020332.2:p.Val134del
XM_011529966.1:c.553_555del	XP_011528268.1:p.Val185del
XM_011529967.1:c.553_555del	XP_011528269.1:p.Val185del
XM_011529968.1:c.553_555del	XP_011528270.1:p.Val185del
XM_011529969.1:c.409_411del	XP_011528271.1:p.Val137del
XM_011529970.1:c.400_402del	XP_011528272.1:p.Val134del
XM_011529971.1:c.409_411del	XP_011528273.1:p.Val137del
XM_011529972.1:c.553_555del	XP_011528274.1:p.Val185del
NM_000106.6:c.553_555del MANE Select	NP_000097.3:p.Val185del
NM_001025161.3:c.400_402del	NP_001020332.2:p.Val134del