Canonical Allele Identifier: CA2662769790

Gene: ICOS

Linked Data

• gnomAD v4: 2-203936960-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936960_203936961insC , CM000664.2:g.203936960_203936961insC	GRCh38
NC_000002.11:g.204801683_204801684insC , CM000664.1:g.204801683_204801684insC	GRCh37
NC_000002.10:g.204509928_204509929insC	NCBI36
NG_011586.1:g.5181_5182insC , LRG_65:g.5181_5182insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+88_58+89insC MANE Select	ENSP00000319476.6:n.58+88_58+89insC
ENST00000316386.10:c.58+88_58+89insC	ENSP00000319476.6:n.58+88_58+89insC
ENST00000435193.1:c.58+88_58+89insC	ENSP00000415951.1:n.58+88_58+89insC
NM_012092.3:c.58+88_58+89insC , LRG_65t1:c.58+88_58+89insC	NP_036224.1:n.58+88_58+89insC
XM_011511028.1:c.58+88_58+89insC	XP_011509330.1:n.58+88_58+89insC
XM_011511030.1:c.-360+88_-360+89insC	XP_011509332.1:n.-360+88_-360+89insC
XM_011511031.1:c.-264+88_-264+89insC	XP_011509333.1:n.-264+88_-264+89insC
XR_427213.2:n.366+356_366+357insG
XR_001739861.1:n.380+356_380+357insG
XR_427213.3:n.380+356_380+357insG
NM_012092.4:c.58+88_58+89insC MANE Select	NP_036224.1:n.58+88_58+89insC