Canonical Allele Identifier: CA2067293

Gene: ICOS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.203956771C>T , CM000664.2:g.203956771C>T	GRCh38
NC_000002.11:g.204821494C>T , CM000664.1:g.204821494C>T	GRCh37
NC_000002.10:g.204529739C>T	NCBI36
NG_011586.1:g.24992C>T , LRG_65:g.24992C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012092.4:c.501+6C>T MANE Select	NP_036224.1:n.501+6C>T
ENST00000316386.11:c.501+6C>T MANE Select	ENSP00000319476.6:n.501+6C>T
NM_012092.3:c.501+6C>T , LRG_65t1:c.501+6C>T	NP_036224.1:n.501+6C>T
ENST00000316386.10:c.501+6C>T	ENSP00000319476.6:n.501+6C>T
ENST00000435193.1:c.501+6C>T	ENSP00000415951.1:n.501+6C>T
XM_011511028.1:c.501+6C>T	XP_011509330.1:n.501+6C>T
XM_011511029.1:c.504+6C>T	XP_011509331.1:n.504+6C>T
XM_011511030.1:c.414+6C>T	XP_011509332.1:n.414+6C>T
XM_011511031.1:c.414+6C>T	XP_011509333.1:n.414+6C>T