Canonical Allele Identifier: CA411769849

Gene: CYP2D6

Linked Data

• MyVariant Identifiers: chr22:g.42522631A>T (hg19) ; chr22:g.42126629A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126629A>T , CM000684.2:g.42126629A>T	GRCh38
NC_000022.10:g.42522631A>T , CM000684.1:g.42522631A>T	GRCh37
NC_000022.9:g.40852575A>T	NCBI36
NG_008376.3:g.8363T>A
NG_008376.4:g.9182T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1237T>A	ENSP00000353241.6:n.1237T>A
ENST00000645361.2:c.1439T>A MANE Select	ENSP00000496150.1:p.Val480Asp
ENST00000359033.4:c.1286T>A	ENSP00000351927.4:p.Val429Asp
ENST00000360124.9:c.1057T>A	ENSP00000353241.5:n.1057T>A
ENST00000360608.9:c.1439T>A	ENSP00000353820.5:p.Val480Asp
ENST00000389970.7:c.1430T>A	ENSP00000374620.4:p.Val477Asp
ENST00000488442.1:n.2163T>A
NM_000106.5:c.1439T>A	NP_000097.3:p.Val480Asp
NM_001025161.2:c.1286T>A	NP_001020332.2:p.Val429Asp
XM_011529966.1:c.1439T>A	XP_011528268.1:p.Val480Asp
XM_011529967.1:c.1439T>A	XP_011528269.1:p.Val480Asp
XM_011529968.1:c.1439T>A	XP_011528270.1:p.Val480Asp
XM_011529969.1:c.1295T>A	XP_011528271.1:p.Val432Asp
XM_011529970.1:c.1286T>A	XP_011528272.1:p.Val429Asp
XM_011529971.1:c.1295T>A	XP_011528273.1:p.Val432Asp
NM_000106.6:c.1439T>A MANE Select	NP_000097.3:p.Val480Asp
NM_001025161.3:c.1286T>A	NP_001020332.2:p.Val429Asp