Canonical Allele Identifier: CA1977130532

Gene: CD6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.60993161T= , CM000673.2:g.60993161T=	GRCh38
NC_000011.9:g.60760633T= , CM000673.1:g.60760633T=	GRCh37
NC_000011.8:g.60517209T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000313421.11:c.50-13413T= MANE Select	ENSP00000323280.7:n.50-13413T=
ENST00000344931.9:c.50-13413T=	ENSP00000340334.5:n.50-13413T=
ENST00000352009.9:c.50-13413T=	ENSP00000340628.5:n.50-13413T=
ENST00000433107.6:c.50-13413T=	ENSP00000410638.2:n.50-13413T=
ENST00000452451.6:c.50-13413T=	ENSP00000390676.2:n.50-13413T=
ENST00000542157.5:c.50-13413T=	ENSP00000440055.1:n.50-13413T=
ENST00000542254.5:c.*78+10391T=	ENSP00000443748.1:n.*78+10391T=
ENST00000545105.5:n.178-13413T=
NM_001254750.1:c.50-13413T=	NP_001241679.1:n.50-13413T=
NM_001254751.1:c.50-13413T=	NP_001241680.1:n.50-13413T=
NM_006725.4:c.50-13413T=	NP_006716.3:n.50-13413T=
NR_045638.1:n.275-13413T=
XM_006718738.1:c.50-13413T=	XP_006718801.1:n.50-13413T=
XM_006718739.1:c.50-13413T=	XP_006718802.1:n.50-13413T=
XM_006718740.1:c.50-13413T=	XP_006718803.1:n.50-13413T=
XM_006718741.1:c.50-13413T=	XP_006718804.1:n.50-13413T=
XM_011545360.1:c.50-13413T=	XP_011543662.1:n.50-13413T=
XM_011545361.1:c.50-13413T=	XP_011543663.1:n.50-13413T=
XM_011545362.1:c.50-13413T=	XP_011543664.1:n.50-13413T=
XM_006718738.2:c.50-13413T=	XP_006718801.1:n.50-13413T=
XM_006718739.2:c.50-13413T=	XP_006718802.1:n.50-13413T=
XM_006718740.2:c.50-13413T=	XP_006718803.1:n.50-13413T=
XM_006718741.2:c.50-13413T=	XP_006718804.1:n.50-13413T=
XM_011545360.2:c.50-13413T=	XP_011543662.1:n.50-13413T=
XM_011545362.2:c.50-13413T=	XP_011543664.1:n.50-13413T=
NM_006725.5:c.50-13413T= MANE Select	NP_006716.3:n.50-13413T=
NM_001254750.2:c.50-13413T=	NP_001241679.1:n.50-13413T=
NM_001254751.2:c.50-13413T=	NP_001241680.1:n.50-13413T=
NR_045638.2:n.236-13413T=