Canonical Allele Identifier: CA377677494

Gene: CYP2C8

Linked Data

• MyVariant Identifiers: chr10:g.96797012A>G (hg19) ; chr10:g.95037255A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037255A>G , CM000672.2:g.95037255A>G	GRCh38
NC_000010.10:g.96797012A>G , CM000672.1:g.96797012A>G	GRCh37
NC_000010.9:g.96787002A>G	NCBI36
NG_007972.1:g.37243T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1346T>C MANE Select	ENSP00000360317.3:p.Leu449Pro
ENST00000371270.5:c.1346T>C	ENSP00000360317.3:p.Leu449Pro
ENST00000490994.6:c.*1132T>C	ENSP00000433314.1:n.*1132T>C
ENST00000525991.5:c.*921T>C	ENSP00000433842.1:n.*921T>C
ENST00000526814.5:n.1601T>C
ENST00000527420.5:c.*203T>C	ENSP00000433191.1:n.*203T>C
ENST00000527953.5:n.1640T>C
ENST00000531714.1:n.534T>C
ENST00000533320.5:n.1580T>C
ENST00000535898.5:c.1040T>C	ENSP00000445062.1:p.Leu347Pro
ENST00000539050.5:c.1136T>C	ENSP00000442343.2:p.Leu379Pro
ENST00000623108.3:c.1136T>C	ENSP00000485110.1:p.Leu379Pro
NM_000770.3:c.1346T>C MANE Select	NP_000761.3:p.Leu449Pro
NM_001198853.1:c.1136T>C	NP_001185782.1:p.Leu379Pro
NM_001198854.1:c.1040T>C	NP_001185783.1:p.Leu347Pro
NM_001198855.1:c.1136T>C	NP_001185784.1:p.Leu379Pro
XR_945610.1:n.1481T>C