Canonical Allele Identifier: CA2842291675

Gene: RCBTB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.49544642T>C , CM000675.2:g.49544642T>C	GRCh38
NC_000013.10:g.50118778T>C , CM000675.1:g.50118778T>C	GRCh37
NC_000013.9:g.49016779T>C	NCBI36
NG_046892.1:g.45965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378302.7:c.1172+95A>G MANE Select	ENSP00000367552.2:n.1172+95A>G
ENST00000258646.3:c.1172+95A>G	ENSP00000258646.3:n.1172+95A>G
ENST00000378302.6:c.1172+95A>G	ENSP00000367552.2:n.1172+95A>G
NM_018191.3:c.1172+95A>G	NP_060661.3:n.1172+95A>G
XM_005266441.2:c.1172+95A>G	XP_005266498.1:n.1172+95A>G
XM_011535133.1:c.1172+95A>G	XP_011533435.1:n.1172+95A>G
XM_011535134.1:c.1172+95A>G	XP_011533436.1:n.1172+95A>G
XM_011535135.1:c.785+95A>G	XP_011533437.1:n.785+95A>G
XR_941613.1:n.3745+95A>G
NM_001352500.1:c.1172+95A>G	NP_001339429.1:n.1172+95A>G
NM_001352501.1:c.1172+95A>G	NP_001339430.1:n.1172+95A>G
NM_001352502.1:c.1172+95A>G	NP_001339431.1:n.1172+95A>G
NM_001352503.1:c.1172+95A>G	NP_001339432.1:n.1172+95A>G
NM_001352504.1:c.1172+95A>G	NP_001339433.1:n.1172+95A>G
NM_001352506.1:c.593+95A>G	NP_001339435.1:n.593+95A>G
NR_148015.1:n.1591+95A>G
NR_148016.1:n.1547+95A>G
XM_011535135.2:c.785+95A>G	XP_011533437.1:n.785+95A>G
XR_001749596.1:n.3094+95A>G
NM_018191.4:c.1172+95A>G MANE Select	NP_060661.3:n.1172+95A>G
NM_001352500.2:c.1172+95A>G	NP_001339429.1:n.1172+95A>G
NM_001352501.2:c.1172+95A>G	NP_001339430.1:n.1172+95A>G
NM_001352502.2:c.1172+95A>G	NP_001339431.1:n.1172+95A>G
NM_001352503.2:c.1172+95A>G	NP_001339432.1:n.1172+95A>G
NM_001352506.2:c.593+95A>G	NP_001339435.1:n.593+95A>G
NR_148015.2:n.1566+95A>G
NR_148016.2:n.1522+95A>G
NM_001352504.2:c.1172+95A>G	NP_001339433.1:n.1172+95A>G