Canonical Allele Identifier: CA1468311880

Gene: CXCL8

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73740952T= , CM000666.2:g.73740952T=	GRCh38
NC_000004.11:g.74606669T= , CM000666.1:g.74606669T=	GRCh37
NC_000004.10:g.74825533T=	NCBI36
NG_029889.1:g.5447T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696131.1:c.*171T=	ENSP00000512424.1:n.*171T=
ENST00000696132.1:c.*22+149T=	ENSP00000512425.1:n.*22+149T=
ENST00000307407.8:c.64+230T= MANE Select	ENSP00000306512.3:n.64+230T=
ENST00000307407.7:c.64+230T=	ENSP00000306512.3:n.64+230T=
ENST00000401931.1:c.64+230T=	ENSP00000385908.1:n.64+230T=
ENST00000483500.1:n.154+230T=
NM_000584.3:c.64+230T=	NP_000575.1:n.64+230T=
NM_001354840.1:c.64+230T=	NP_001341769.1:n.64+230T=
NM_000584.4:c.64+230T= MANE Select	NP_000575.1:n.64+230T=
NM_001354840.2:c.64+230T=	NP_001341769.1:n.64+230T=
NM_001354840.3:c.64+230T=	NP_001341769.1:n.64+230T=