Canonical Allele Identifier: CA377677495

Gene: CYP2C8

Linked Data

• gnomAD v4: 10-95037255-A-T
• MyVariant Identifiers: chr10:g.96797012A>T (hg19) ; chr10:g.95037255A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1346T>A MANE Select	ENSP00000360317.3:p.Leu449Gln
ENST00000371270.5:c.1346T>A	ENSP00000360317.3:p.Leu449Gln
ENST00000490994.6:c.*1132T>A	ENSP00000433314.1:n.*1132T>A
ENST00000525991.5:c.*921T>A	ENSP00000433842.1:n.*921T>A
ENST00000526814.5:n.1601T>A
ENST00000527420.5:c.*203T>A	ENSP00000433191.1:n.*203T>A
ENST00000527953.5:n.1640T>A
ENST00000531714.1:n.534T>A
ENST00000533320.5:n.1580T>A
ENST00000535898.5:c.1040T>A	ENSP00000445062.1:p.Leu347Gln
ENST00000539050.5:c.1136T>A	ENSP00000442343.2:p.Leu379Gln
ENST00000623108.3:c.1136T>A	ENSP00000485110.1:p.Leu379Gln
NM_000770.3:c.1346T>A MANE Select	NP_000761.3:p.Leu449Gln
NM_001198853.1:c.1136T>A	NP_001185782.1:p.Leu379Gln
NM_001198854.1:c.1040T>A	NP_001185783.1:p.Leu347Gln
NM_001198855.1:c.1136T>A	NP_001185784.1:p.Leu379Gln
XR_945610.1:n.1481T>A