Canonical Allele Identifier: CA647763515

Gene: ICOS

Linked Data

• COSMIC: COSN19705340

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936945A>C , CM000664.2:g.203936945A>C	GRCh38
NC_000002.11:g.204801668A>C , CM000664.1:g.204801668A>C	GRCh37
NC_000002.10:g.204509913A>C	NCBI36
NG_011586.1:g.5166A>C , LRG_65:g.5166A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000316386.11:c.58+73A>C MANE Select	ENSP00000319476.6:n.58+73A>C
ENST00000316386.10:c.58+73A>C	ENSP00000319476.6:n.58+73A>C
ENST00000435193.1:c.58+73A>C	ENSP00000415951.1:n.58+73A>C
NM_012092.3:c.58+73A>C , LRG_65t1:c.58+73A>C	NP_036224.1:n.58+73A>C
XM_011511028.1:c.58+73A>C	XP_011509330.1:n.58+73A>C
XM_011511030.1:c.-360+73A>C	XP_011509332.1:n.-360+73A>C
XM_011511031.1:c.-264+73A>C	XP_011509333.1:n.-264+73A>C
XR_427213.2:n.366+372T>G
XR_001739861.1:n.380+372T>G
XR_427213.3:n.380+372T>G
NM_012092.4:c.58+73A>C MANE Select	NP_036224.1:n.58+73A>C