Canonical Allele Identifier: CA595332961

Gene: CYP2C8

Linked Data

• dbSNP Id: rs1441417470
• gnomAD v2: 10-96796976-A-AATCTTCC
• MyVariant Identifiers: chr10:g.96796976_96796977insATCTTCC (hg19) ; chr10:g.95037219_95037220insATCTTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.95037219_95037220insATCTTCC , CM000672.2:g.95037219_95037220insATCTTCC	GRCh38
NC_000010.10:g.96796976_96796977insATCTTCC , CM000672.1:g.96796976_96796977insATCTTCC	GRCh37
NC_000010.9:g.96786966_96786967insATCTTCC	NCBI36
NG_007972.1:g.37278_37279insGGAAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371270.6:c.1381_1382insGGAAGAT MANE Select	ENSP00000360317.3:p.Val461GlyfsTer4
ENST00000371270.5:c.1381_1382insGGAAGAT	ENSP00000360317.3:p.Val461GlyfsTer4
ENST00000490994.6:c.*1167_*1168insGGAAGAT	ENSP00000433314.1:n.*1167_*1168insGGAAGAT
ENST00000525991.5:c.*956_*957insGGAAGAT	ENSP00000433842.1:n.*956_*957insGGAAGAT
ENST00000526814.5:n.1636_1637insGGAAGAT
ENST00000527420.5:c.*238_*239insGGAAGAT	ENSP00000433191.1:n.*238_*239insGGAAGAT
ENST00000527953.5:n.1675_1676insGGAAGAT
ENST00000531714.1:n.569_570insGGAAGAT
ENST00000533320.5:n.1615_1616insGGAAGAT
ENST00000535898.5:c.1075_1076insGGAAGAT	ENSP00000445062.1:p.Val359GlyfsTer4
ENST00000539050.5:c.1171_1172insGGAAGAT	ENSP00000442343.2:p.Val391GlyfsTer4
ENST00000623108.3:c.1171_1172insGGAAGAT	ENSP00000485110.1:p.Val391GlyfsTer4
NM_000770.3:c.1381_1382insGGAAGAT MANE Select	NP_000761.3:p.Val461GlyfsTer4
NM_001198853.1:c.1171_1172insGGAAGAT	NP_001185782.1:p.Val391GlyfsTer4
NM_001198854.1:c.1075_1076insGGAAGAT	NP_001185783.1:p.Val359GlyfsTer4
NM_001198855.1:c.1171_1172insGGAAGAT	NP_001185784.1:p.Val391GlyfsTer4
XR_945610.1:n.1516_1517insGGAAGAT