Canonical Allele Identifier: CA2662769792

Gene: ICOS

Linked Data

• gnomAD v4: 2-203936964-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203936964A>T , CM000664.2:g.203936964A>T	GRCh38
NC_000002.11:g.204801687A>T , CM000664.1:g.204801687A>T	GRCh37
NC_000002.10:g.204509932A>T	NCBI36
NG_011586.1:g.5185A>T , LRG_65:g.5185A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.58+92A>T MANE Select	ENSP00000319476.6:n.58+92A>T
ENST00000316386.10:c.58+92A>T	ENSP00000319476.6:n.58+92A>T
ENST00000435193.1:c.58+92A>T	ENSP00000415951.1:n.58+92A>T
NM_012092.3:c.58+92A>T , LRG_65t1:c.58+92A>T	NP_036224.1:n.58+92A>T
XM_011511028.1:c.58+92A>T	XP_011509330.1:n.58+92A>T
XM_011511030.1:c.-360+92A>T	XP_011509332.1:n.-360+92A>T
XM_011511031.1:c.-264+92A>T	XP_011509333.1:n.-264+92A>T
XR_427213.2:n.366+353T>A
XR_001739861.1:n.380+353T>A
XR_427213.3:n.380+353T>A
NM_012092.4:c.58+92A>T MANE Select	NP_036224.1:n.58+92A>T