Canonical Allele Identifier: CA1322178667

Gene: ICOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936950C= , CM000664.2:g.203936950C=	GRCh38
NC_000002.11:g.204801673C= , CM000664.1:g.204801673C=	GRCh37
NC_000002.10:g.204509918C=	NCBI36
NG_011586.1:g.5171C= , LRG_65:g.5171C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+78C= MANE Select	ENSP00000319476.6:n.58+78C=
ENST00000316386.10:c.58+78C=	ENSP00000319476.6:n.58+78C=
ENST00000435193.1:c.58+78C=	ENSP00000415951.1:n.58+78C=
NM_012092.3:c.58+78C= , LRG_65t1:c.58+78C=	NP_036224.1:n.58+78C=
XM_011511028.1:c.58+78C=	XP_011509330.1:n.58+78C=
XM_011511030.1:c.-360+78C=	XP_011509332.1:n.-360+78C=
XM_011511031.1:c.-264+78C=	XP_011509333.1:n.-264+78C=
XR_427213.2:n.366+367G=
XR_001739861.1:n.380+367G=
XR_427213.3:n.380+367G=
NM_012092.4:c.58+78C= MANE Select	NP_036224.1:n.58+78C=