Canonical Allele Identifier: CA128722

Gene: CD4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6816241C>T , CM000674.2:g.6816241C>T	GRCh38
NC_000012.11:g.6925407C>T , CM000674.1:g.6925407C>T	GRCh37
NC_000012.10:g.6795668C>T	NCBI36
NG_027688.1:g.31770C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000616.5:c.793C>T MANE Select	NP_000607.1:p.Arg265Trp
ENST00000011653.9:c.793C>T MANE Select	ENSP00000011653.4:p.Arg265Trp
NM_000616.4:c.793C>T	NP_000607.1:p.Arg265Trp
NM_001195014.2:c.256C>T	NP_001181943.1:p.Arg86Trp
NM_001195014.3:c.256C>T	NP_001181943.1:p.Arg86Trp
NM_001195015.2:c.-27C>T	NP_001181944.1:n.-27C>T
NM_001195015.3:c.-27C>T	NP_001181944.1:n.-27C>T
NM_001195016.2:c.-27C>T	NP_001181945.1:n.-27C>T
NM_001195016.3:c.-27C>T	NP_001181945.1:n.-27C>T
NM_001195017.2:c.-27C>T	NP_001181946.1:n.-27C>T
NM_001195017.3:c.-27C>T	NP_001181946.1:n.-27C>T
NM_001382705.1:c.-27C>T	NP_001369634.1:n.-27C>T
NM_001382706.1:c.-27C>T	NP_001369635.1:n.-27C>T
NM_001382707.1:c.793C>T	NP_001369636.1:p.Arg265Trp
NM_001382714.1:c.628C>T	NP_001369643.1:p.Arg210Trp
ENST00000011653.8:c.793C>T	ENSP00000011653.4:p.Arg265Trp
ENST00000437800.6:n.1031C>T
ENST00000538827.5:n.869C>T
ENST00000541982.5:c.*506C>T	ENSP00000445167.1:n.*506C>T
XM_011521039.1:c.256C>T	XP_011519341.1:p.Arg86Trp
XM_017020228.2:c.-27C>T	XP_016875717.1:n.-27C>T