Canonical Allele Identifier: CA2090496439

Gene: RCBTB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.49544567G= , CM000675.2:g.49544567G=	GRCh38
NC_000013.10:g.50118703G= , CM000675.1:g.50118703G=	GRCh37
NC_000013.9:g.49016704G=	NCBI36
NG_046892.1:g.46040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378302.7:c.1172+170C= MANE Select	ENSP00000367552.2:n.1172+170C=
ENST00000258646.3:c.1172+170C=	ENSP00000258646.3:n.1172+170C=
ENST00000378302.6:c.1172+170C=	ENSP00000367552.2:n.1172+170C=
NM_018191.3:c.1172+170C=	NP_060661.3:n.1172+170C=
XM_005266441.2:c.1172+170C=	XP_005266498.1:n.1172+170C=
XM_011535133.1:c.1172+170C=	XP_011533435.1:n.1172+170C=
XM_011535134.1:c.1172+170C=	XP_011533436.1:n.1172+170C=
XM_011535135.1:c.785+170C=	XP_011533437.1:n.785+170C=
XR_941613.1:n.3745+170C=
NM_001352500.1:c.1172+170C=	NP_001339429.1:n.1172+170C=
NM_001352501.1:c.1172+170C=	NP_001339430.1:n.1172+170C=
NM_001352502.1:c.1172+170C=	NP_001339431.1:n.1172+170C=
NM_001352503.1:c.1172+170C=	NP_001339432.1:n.1172+170C=
NM_001352504.1:c.1172+170C=	NP_001339433.1:n.1172+170C=
NM_001352506.1:c.593+170C=	NP_001339435.1:n.593+170C=
NR_148015.1:n.1591+170C=
NR_148016.1:n.1547+170C=
XM_011535135.2:c.785+170C=	XP_011533437.1:n.785+170C=
XR_001749596.1:n.3094+170C=
NM_018191.4:c.1172+170C= MANE Select	NP_060661.3:n.1172+170C=
NM_001352500.2:c.1172+170C=	NP_001339429.1:n.1172+170C=
NM_001352501.2:c.1172+170C=	NP_001339430.1:n.1172+170C=
NM_001352502.2:c.1172+170C=	NP_001339431.1:n.1172+170C=
NM_001352503.2:c.1172+170C=	NP_001339432.1:n.1172+170C=
NM_001352506.2:c.593+170C=	NP_001339435.1:n.593+170C=
NR_148015.2:n.1566+170C=
NR_148016.2:n.1522+170C=
NM_001352504.2:c.1172+170C=	NP_001339433.1:n.1172+170C=