Canonical Allele Identifier: CA377682883

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96827019C>A (hg19) ; chr10:g.95067262C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95067262C>A , CM000672.2:g.95067262C>A	GRCh38
NC_000010.10:g.96827019C>A , CM000672.1:g.96827019C>A	GRCh37
NC_000010.9:g.96817009C>A	NCBI36
NG_007972.1:g.7236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.427G>T MANE Select	ENSP00000360317.3:p.Asp143Tyr
ENST00000371270.5:c.427G>T	ENSP00000360317.3:p.Asp143Tyr
ENST00000479946.2:n.731G>T
ENST00000490994.6:c.*213G>T	ENSP00000433314.1:n.*213G>T
ENST00000525991.5:c.*2G>T	ENSP00000433842.1:n.*2G>T
ENST00000526814.5:n.682G>T
ENST00000527420.5:c.427G>T	ENSP00000433191.1:p.Asp143Tyr
ENST00000527953.5:n.682G>T
ENST00000533320.5:n.661G>T
ENST00000535898.5:c.121G>T	ENSP00000445062.1:p.Asp41Tyr
ENST00000539050.5:c.217G>T	ENSP00000442343.2:p.Asp73Tyr
ENST00000623108.3:c.217G>T	ENSP00000485110.1:p.Asp73Tyr
ENST00000628935.1:c.169G>T	ENSP00000487145.1:p.Asp57Tyr
NM_000770.3:c.427G>T MANE Select	NP_000761.3:p.Asp143Tyr
NM_001198853.1:c.217G>T	NP_001185782.1:p.Asp73Tyr
NM_001198854.1:c.121G>T	NP_001185783.1:p.Asp41Tyr
NM_001198855.1:c.217G>T	NP_001185784.1:p.Asp73Tyr
XR_945610.1:n.523G>T