Canonical Allele Identifier: CA1468312103

Gene: CXCL8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73741338C= , CM000666.2:g.73741338C=	GRCh38
NC_000004.11:g.74607055C= , CM000666.1:g.74607055C=	GRCh37
NC_000004.10:g.74825919C=	NCBI36
NG_029889.1:g.5833C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000584.4:c.65-204C= MANE Select	NP_000575.1:n.65-204C=
ENST00000307407.8:c.65-204C= MANE Select	ENSP00000306512.3:n.65-204C=
NM_000584.3:c.65-204C=	NP_000575.1:n.65-204C=
NM_001354840.1:c.65-204C=	NP_001341769.1:n.65-204C=
NM_001354840.2:c.65-204C=	NP_001341769.1:n.65-204C=
NM_001354840.3:c.65-204C=	NP_001341769.1:n.65-204C=
ENST00000307407.7:c.65-204C=	ENSP00000306512.3:n.65-204C=
ENST00000401931.1:c.65-204C=	ENSP00000385908.1:n.65-204C=
ENST00000483500.1:n.155-204C=
ENST00000696131.1:c.*269-204C=	ENSP00000512424.1:n.*269-204C=
ENST00000696132.1:c.*23-204C=	ENSP00000512425.1:n.*23-204C=