Canonical Allele Identifier: CA2014254933

Gene: CD4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6800276T>G , CM000674.2:g.6800276T>G	GRCh38
NC_000012.11:g.6909442T>G , CM000674.1:g.6909442T>G	GRCh37
NC_000012.10:g.6779703T>G	NCBI36
NG_027688.1:g.15805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000011653.9:c.50-31T>G MANE Select	ENSP00000011653.4:n.50-31T>G
ENST00000011653.8:c.50-31T>G	ENSP00000011653.4:n.50-31T>G
ENST00000437800.6:n.127+10614T>G
ENST00000535466.5:n.438-31T>G
ENST00000535707.5:n.439-31T>G
ENST00000536590.1:n.280-31T>G
ENST00000536610.5:n.352-31T>G
ENST00000538827.5:n.127+10614T>G
ENST00000539492.1:c.50-31T>G	ENSP00000440720.1:n.50-31T>G
ENST00000541982.5:c.49+89T>G	ENSP00000445167.1:n.49+89T>G
ENST00000544344.5:n.127+10614T>G
NM_000616.4:c.50-31T>G	NP_000607.1:n.50-31T>G
NM_001195014.2:c.-649+10614T>G	NP_001181943.1:n.-649+10614T>G
NM_001195015.2:c.-619+10614T>G	NP_001181944.1:n.-619+10614T>G
NM_001195016.2:c.-606+10614T>G	NP_001181945.1:n.-606+10614T>G
NM_001195017.2:c.-584+10614T>G	NP_001181946.1:n.-584+10614T>G
XM_011521039.1:c.-812+10614T>G	XP_011519341.1:n.-812+10614T>G
XM_017020228.2:c.-769+10614T>G	XP_016875717.1:n.-769+10614T>G
NM_000616.5:c.50-31T>G MANE Select	NP_000607.1:n.50-31T>G
NM_001195014.3:c.-649+10614T>G	NP_001181943.1:n.-649+10614T>G
NM_001195015.3:c.-619+10614T>G	NP_001181944.1:n.-619+10614T>G
NM_001195016.3:c.-606+10614T>G	NP_001181945.1:n.-606+10614T>G
NM_001195017.3:c.-584+10614T>G	NP_001181946.1:n.-584+10614T>G
NM_001382705.1:c.-769+10614T>G	NP_001369634.1:n.-769+10614T>G
NM_001382706.1:c.-933-31T>G	NP_001369635.1:n.-933-31T>G
NM_001382707.1:c.50-31T>G	NP_001369636.1:n.50-31T>G
NM_001382714.1:c.49+89T>G	NP_001369643.1:n.49+89T>G