Canonical Allele Identifier: CA1322178668

Gene: ICOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936951G= , CM000664.2:g.203936951G=	GRCh38
NC_000002.11:g.204801674G= , CM000664.1:g.204801674G=	GRCh37
NC_000002.10:g.204509919G=	NCBI36
NG_011586.1:g.5172G= , LRG_65:g.5172G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+79G= MANE Select	ENSP00000319476.6:n.58+79G=
ENST00000316386.10:c.58+79G=	ENSP00000319476.6:n.58+79G=
ENST00000435193.1:c.58+79G=	ENSP00000415951.1:n.58+79G=
NM_012092.3:c.58+79G= , LRG_65t1:c.58+79G=	NP_036224.1:n.58+79G=
XM_011511028.1:c.58+79G=	XP_011509330.1:n.58+79G=
XM_011511030.1:c.-360+79G=	XP_011509332.1:n.-360+79G=
XM_011511031.1:c.-264+79G=	XP_011509333.1:n.-264+79G=
XR_427213.2:n.366+366C=
XR_001739861.1:n.380+366C=
XR_427213.3:n.380+366C=
NM_012092.4:c.58+79G= MANE Select	NP_036224.1:n.58+79G=