Canonical Allele Identifier: CA380641899
Gene: CD6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61009629T>A , CM000673.2:g.61009629T>A GRCh38
NC_000011.9:g.60777101T>A , CM000673.1:g.60777101T>A GRCh37
NC_000011.8:g.60533677T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000313421.11:c.839T>A MANE Select ENSP00000323280.7:p.Val280Glu
ENST00000344931.9:c.839T>A ENSP00000340334.5:p.Val280Glu
ENST00000352009.9:c.839T>A ENSP00000340628.5:p.Val280Glu
ENST00000433107.6:c.781+784T>A ENSP00000410638.2:n.781+784T>A
ENST00000452451.6:c.839T>A ENSP00000390676.2:p.Val280Glu
ENST00000538611.1:c.312+784T>A
ENST00000541964.1:n.553T>A
ENST00000542157.5:c.781+784T>A ENSP00000440055.1:n.781+784T>A
ENST00000545105.5:n.247-218T>A
NM_001254750.1:c.839T>A NP_001241679.1:p.Val280Glu
NM_001254751.1:c.839T>A NP_001241680.1:p.Val280Glu
NM_006725.4:c.839T>A NP_006716.3:p.Val280Glu
NR_045638.1:n.1064T>A
XM_006718738.1:c.839T>A XP_006718801.1:p.Val280Glu
XM_006718739.1:c.839T>A XP_006718802.1:p.Val280Glu
XM_006718740.1:c.839T>A XP_006718803.1:p.Val280Glu
XM_006718741.1:c.839T>A XP_006718804.1:p.Val280Glu
XM_011545360.1:c.839T>A XP_011543662.1:p.Val280Glu
XM_011545361.1:c.839T>A XP_011543663.1:p.Val280Glu
XM_011545362.1:c.781+784T>A XP_011543664.1:n.781+784T>A
XM_006718738.2:c.839T>A XP_006718801.1:p.Val280Glu
XM_006718739.2:c.839T>A XP_006718802.1:p.Val280Glu
XM_006718740.2:c.839T>A XP_006718803.1:p.Val280Glu
XM_006718741.2:c.839T>A XP_006718804.1:p.Val280Glu
XM_011545360.2:c.839T>A XP_011543662.1:p.Val280Glu
XM_011545362.2:c.781+784T>A XP_011543664.1:n.781+784T>A
NM_006725.5:c.839T>A MANE Select NP_006716.3:p.Val280Glu
NM_001254750.2:c.839T>A NP_001241679.1:p.Val280Glu
NM_001254751.2:c.839T>A NP_001241680.1:p.Val280Glu
NR_045638.2:n.1025T>A