Canonical Allele Identifier: CA595638965

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1434821194
• gnomAD v2: 10-96826980-ACTC-A
• gnomAD v3: 10-95067223-ACTC-A
• gnomAD v4: 10-95067223-ACTC-A
• MyVariant Identifiers: chr10:g.96826981_96826983del (hg19) ; chr10:g.95067224_95067226del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067228_95067230del , CM000672.2:g.95067228_95067230del	GRCh38
NC_000010.10:g.96826985_96826987del , CM000672.1:g.96826985_96826987del	GRCh37
NC_000010.9:g.96816975_96816977del	NCBI36
NG_007972.1:g.7272_7274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.463_465del MANE Select	ENSP00000360317.3:p.Glu155del
ENST00000371270.5:c.463_465del	ENSP00000360317.3:p.Glu155del
ENST00000479946.2:n.767_769del
ENST00000490994.6:c.*249_*251del	ENSP00000433314.1:n.*249_*251del
ENST00000525991.5:c.*38_*40del	ENSP00000433842.1:n.*38_*40del
ENST00000526814.5:n.718_720del
ENST00000527420.5:c.463_465del	ENSP00000433191.1:p.Glu155del
ENST00000527953.5:n.718_720del
ENST00000533320.5:n.697_699del
ENST00000535898.5:c.157_159del	ENSP00000445062.1:p.Glu53del
ENST00000539050.5:c.253_255del	ENSP00000442343.2:p.Glu85del
ENST00000623108.3:c.253_255del	ENSP00000485110.1:p.Glu85del
ENST00000628935.1:c.205_207del	ENSP00000487145.1:p.Glu69del
NM_000770.3:c.463_465del MANE Select	NP_000761.3:p.Glu155del
NM_001198853.1:c.253_255del	NP_001185782.1:p.Glu85del
NM_001198854.1:c.157_159del	NP_001185783.1:p.Glu53del
NM_001198855.1:c.253_255del	NP_001185784.1:p.Glu85del
XR_945610.1:n.559_561del