Canonical Allele Identifier: CA10265051

Gene: CYP2D6

Linked Data

• dbSNP Id: rs72549356
• ExAC: 22:42524929 T / TGGGGCGAAAGGGGCGAAA
• gnomAD v2: 22-42524929-T-TGGGGCGAAAGGGGCGAAA
• gnomAD v3: 22-42128927-T-TGGGGCGAAAGGGGCGAAA
• gnomAD v4: 22-42128927-T-TGGGGCGAAAGGGGCGAAA
• MyVariant Identifiers: chr22:g.42524929_42524930insGGGGCGAAAGGGGCGAAA (hg19) ; chr22:g.42128927_42128928insGGGGCGAAAGGGGCGAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128942_42128943insAAAGGGGCGAAAGGGGCG , CM000684.2:g.42128942_42128943insAAAGGGGCGAAAGGGGCG	GRCh38
NC_000022.10:g.42524944_42524945insAAAGGGGCGAAAGGGGCG , CM000684.1:g.42524944_42524945insAAAGGGGCGAAAGGGGCG	GRCh37
NC_000022.9:g.40854888_40854889insAAAGGGGCGAAAGGGGCG	NCBI36
NG_008376.3:g.6064_6065insTTTCGCCCCTTTCGCCCC
NG_008376.4:g.6883_6884insTTTCGCCCCTTTCGCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.369_370insTTTCGCCCCTTTCGCCCC	ENSP00000353241.6:p.Pro123_Asn124insPheArgProPheArgPro
ENST00000645361.2:c.522_523insTTTCGCCCCTTTCGCCCC MANE Select	ENSP00000496150.1:p.Pro174_Asn175insPheArgProPheArgPro
ENST00000359033.4:c.369_370insTTTCGCCCCTTTCGCCCC	ENSP00000351927.4:p.Pro123_Asn124insPheArgProPheArgPro
ENST00000360124.9:c.189_190insTTTCGCCCCTTTCGCCCC	ENSP00000353241.5:p.Pro63_Asn64insPheArgProPheArgPro
ENST00000360608.9:c.522_523insTTTCGCCCCTTTCGCCCC	ENSP00000353820.5:p.Pro174_Asn175insPheArgProPheArgPro
ENST00000389970.7:c.456_457insTTTCGCCCCTTTCGCCCC	ENSP00000374620.4:p.Pro152_Asn153insPheArgProPheArgPro
ENST00000488442.1:n.1246_1247insTTTCGCCCCTTTCGCCCC
NM_000106.5:c.522_523insTTTCGCCCCTTTCGCCCC	NP_000097.3:p.Pro174_Asn175insPheArgProPheArgPro
NM_001025161.2:c.369_370insTTTCGCCCCTTTCGCCCC	NP_001020332.2:p.Pro123_Asn124insPheArgProPheArgPro
XM_011529966.1:c.522_523insTTTCGCCCCTTTCGCCCC	XP_011528268.1:p.Pro174_Asn175insPheArgProPheArgPro
XM_011529967.1:c.522_523insTTTCGCCCCTTTCGCCCC	XP_011528269.1:p.Pro174_Asn175insPheArgProPheArgPro
XM_011529968.1:c.522_523insTTTCGCCCCTTTCGCCCC	XP_011528270.1:p.Pro174_Asn175insPheArgProPheArgPro
XM_011529969.1:c.378_379insTTTCGCCCCTTTCGCCCC	XP_011528271.1:p.Pro126_Asn127insPheArgProPheArgPro
XM_011529970.1:c.369_370insTTTCGCCCCTTTCGCCCC	XP_011528272.1:p.Pro123_Asn124insPheArgProPheArgPro
XM_011529971.1:c.378_379insTTTCGCCCCTTTCGCCCC	XP_011528273.1:p.Pro126_Asn127insPheArgProPheArgPro
XM_011529972.1:c.522_523insTTTCGCCCCTTTCGCCCC	XP_011528274.1:p.Pro174_Asn175insPheArgProPheArgPro
NM_000106.6:c.522_523insTTTCGCCCCTTTCGCCCC MANE Select	NP_000097.3:p.Pro174_Asn175insPheArgProPheArgPro
NM_001025161.3:c.369_370insTTTCGCCCCTTTCGCCCC	NP_001020332.2:p.Pro123_Asn124insPheArgProPheArgPro