Canonical Allele Identifier: CA918736892

Gene: CYP2C9

Linked Data

• dbSNP Id: rs1589405201

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942058_94942059insTTTCAGGCCAAAATACA , CM000672.2:g.94942058_94942059insTTTCAGGCCAAAATACA	GRCh38
NC_000010.10:g.96701815_96701816insTTTCAGGCCAAAATACA , CM000672.1:g.96701815_96701816insTTTCAGGCCAAAATACA	GRCh37
NC_000010.9:g.96691805_96691806insTTTCAGGCCAAAATACA	NCBI36
NG_008385.1:g.8401_8402insTTTCAGGCCAAAATACA
NG_008385.2:g.8901_8902insTTTCAGGCCAAAATACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.331+38_331+39insTTTCAGGCCAAAATACA MANE Select	ENSP00000260682.6:n.331+38_331+39insTTTCAGGCCAAAATACA
ENST00000643112.1:c.331+38_331+39insTTTCAGGCCAAAATACA	ENSP00000496202.1:n.331+38_331+39insTTTCAGGCCAAAATACA
ENST00000645207.1:n.484+38_484+39insTTTCAGGCCAAAATACA
ENST00000260682.6:c.331+38_331+39insTTTCAGGCCAAAATACA	ENSP00000260682.6:n.331+38_331+39insTTTCAGGCCAAAATACA
ENST00000461906.1:n.356+38_356+39insTTTCAGGCCAAAATACA
ENST00000473496.1:n.102+38_102+39insTTTCAGGCCAAAATACA
NM_000771.3:c.331+38_331+39insTTTCAGGCCAAAATACA	NP_000762.2:n.331+38_331+39insTTTCAGGCCAAAATACA
NM_000771.4:c.331+38_331+39insTTTCAGGCCAAAATACA MANE Select	NP_000762.2:n.331+38_331+39insTTTCAGGCCAAAATACA