Canonical Allele Identifier: CA2657029108

Gene: CYP2D6

Linked Data

• gnomAD v4: 22-42126534-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126537_42126538del , CM000684.2:g.42126537_42126538del	GRCh38
NC_000022.10:g.42522539_42522540del , CM000684.1:g.42522539_42522540del	GRCh37
NC_000022.9:g.40852483_40852484del	NCBI36
NG_008376.3:g.8456_8457del
NG_008376.4:g.9275_9276del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1330_1331del	ENSP00000353241.6:n.1330_1331del
ENST00000645361.2:c.*38_*39del MANE Select	ENSP00000496150.1:n.*38_*39del
ENST00000360124.9:c.1150_1151del	ENSP00000353241.5:n.1150_1151del
ENST00000360608.9:c.*38_*39del	ENSP00000353820.5:n.*38_*39del
ENST00000389970.7:c.*38_*39del	ENSP00000374620.4:n.*38_*39del
ENST00000488442.1:n.2256_2257del
NM_000106.5:c.*38_*39del	NP_000097.3:n.*38_*39del
NM_001025161.2:c.*38_*39del	NP_001020332.2:n.*38_*39del
XM_011529966.1:c.1452+80_1452+81del	XP_011528268.1:n.1452+80_1452+81del
XM_011529967.1:c.1452+80_1452+81del	XP_011528269.1:n.1452+80_1452+81del
XM_011529968.1:c.1452+80_1452+81del	XP_011528270.1:n.1452+80_1452+81del
XM_011529969.1:c.1308+80_1308+81del	XP_011528271.1:n.1308+80_1308+81del
XM_011529970.1:c.1299+80_1299+81del	XP_011528272.1:n.1299+80_1299+81del
XM_011529971.1:c.*38_*39del	XP_011528273.1:n.*38_*39del
NM_000106.6:c.*38_*39del MANE Select	NP_000097.3:n.*38_*39del
NM_001025161.3:c.*38_*39del	NP_001020332.2:n.*38_*39del