Canonical Allele Identifier: CA595333015

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1204707465
• gnomAD v2: 10-96797164-ATAAT-A
• gnomAD v3: 10-95037407-ATAAT-A
• gnomAD v4: 10-95037407-ATAAT-A
• MyVariant Identifiers: chr10:g.96797165_96797168del (hg19) ; chr10:g.95037408_95037411del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037409_95037412del , CM000672.2:g.95037409_95037412del	GRCh38
NC_000010.10:g.96797166_96797169del , CM000672.1:g.96797166_96797169del	GRCh37
NC_000010.9:g.96787156_96787159del	NCBI36
NG_007972.1:g.37087_37090del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1292-102_1292-99del MANE Select	ENSP00000360317.3:n.1292-102_1292-99del
ENST00000371270.5:c.1292-102_1292-99del	ENSP00000360317.3:n.1292-102_1292-99del
ENST00000490994.6:c.*1078-102_*1078-99del	ENSP00000433314.1:n.*1078-102_*1078-99del
ENST00000525991.5:c.*867-102_*867-99del	ENSP00000433842.1:n.*867-102_*867-99del
ENST00000526814.5:n.1547-102_1547-99del
ENST00000527420.5:c.*149-102_*149-99del	ENSP00000433191.1:n.*149-102_*149-99del
ENST00000527953.5:n.1586-102_1586-99del
ENST00000531714.1:n.480-102_480-99del
ENST00000533320.5:n.1526-102_1526-99del
ENST00000535898.5:c.986-102_986-99del	ENSP00000445062.1:n.986-102_986-99del
ENST00000539050.5:c.1082-102_1082-99del	ENSP00000442343.2:n.1082-102_1082-99del
ENST00000623108.3:c.1082-102_1082-99del	ENSP00000485110.1:n.1082-102_1082-99del
NM_000770.3:c.1292-102_1292-99del MANE Select	NP_000761.3:n.1292-102_1292-99del
NM_001198853.1:c.1082-102_1082-99del	NP_001185782.1:n.1082-102_1082-99del
NM_001198854.1:c.986-102_986-99del	NP_001185783.1:n.986-102_986-99del
NM_001198855.1:c.1082-102_1082-99del	NP_001185784.1:n.1082-102_1082-99del
XR_945610.1:n.1427-102_1427-99del