Canonical Allele Identifier: CA763563145

Gene: ICOS

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203954121G>C , CM000664.2:g.203954121G>C	GRCh38
NC_000002.11:g.204818844G>C , CM000664.1:g.204818844G>C	GRCh37
NC_000002.10:g.204527089G>C	NCBI36
NG_011586.1:g.22342G>C , LRG_65:g.22342G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316386.11:c.59-1515G>C MANE Select	ENSP00000319476.6:n.59-1515G>C
ENST00000316386.10:c.59-1515G>C	ENSP00000319476.6:n.59-1515G>C
ENST00000435193.1:c.59-1515G>C	ENSP00000415951.1:n.59-1515G>C
NM_012092.3:c.59-1515G>C , LRG_65t1:c.59-1515G>C	NP_036224.1:n.59-1515G>C
XM_011511028.1:c.59-1515G>C	XP_011509330.1:n.59-1515G>C
XM_011511029.1:c.62-1515G>C	XP_011509331.1:n.62-1515G>C
XM_011511030.1:c.-29-1515G>C	XP_011509332.1:n.-29-1515G>C
XM_011511031.1:c.-29-1515G>C	XP_011509333.1:n.-29-1515G>C
NM_012092.4:c.59-1515G>C MANE Select	NP_036224.1:n.59-1515G>C