Canonical Allele Identifier: CA843409129

Gene: RUNDC3B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87714707G>T , CM000669.2:g.87714707G>T	GRCh38
NC_000007.13:g.87344023G>T , CM000669.1:g.87344023G>T	GRCh37
NC_000007.12:g.87181959G>T	NCBI36
NG_011513.1:g.3542C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394654.4:c.458+4052G>T MANE Select	ENSP00000378149.3:n.458+4052G>T
ENST00000312373.12:n.225+4052G>T
ENST00000338056.7:c.509+4052G>T	ENSP00000337732.3:n.509+4052G>T
ENST00000394654.3:c.458+4052G>T	ENSP00000378149.3:n.458+4052G>T
ENST00000466676.5:n.453+4052G>T
ENST00000489461.5:n.415+4052G>T
ENST00000493037.5:c.458+4052G>T	ENSP00000420394.1:n.458+4052G>T
ENST00000496000.1:n.344+4052G>T
NM_001134405.1:c.458+4052G>T	NP_001127877.1:n.458+4052G>T
NM_001134406.1:c.458+4052G>T	NP_001127878.1:n.458+4052G>T
NM_138290.2:c.509+4052G>T	NP_612147.1:n.509+4052G>T
XM_005250156.2:c.458+4052G>T	XP_005250213.1:n.458+4052G>T
XM_005250158.2:c.98+4052G>T	XP_005250215.1:n.98+4052G>T
XM_011515826.1:c.509+4052G>T	XP_011514128.1:n.509+4052G>T
XM_011515827.1:c.509+4052G>T	XP_011514129.1:n.509+4052G>T
XM_011515828.1:c.116+4052G>T	XP_011514130.1:n.116+4052G>T
XM_011515829.1:c.116+4052G>T	XP_011514131.1:n.116+4052G>T
XM_011515828.2:c.116+4052G>T	XP_011514130.1:n.116+4052G>T
XM_011515829.2:c.116+4052G>T	XP_011514131.1:n.116+4052G>T
XM_017011761.2:c.116+4052G>T	XP_016867250.1:n.116+4052G>T
XM_017011762.1:c.116+4052G>T	XP_016867251.1:n.116+4052G>T
XM_017011763.2:c.116+4052G>T	XP_016867252.1:n.116+4052G>T
XM_017011764.1:c.98+4052G>T	XP_016867253.1:n.98+4052G>T
XM_017011765.2:c.116+4052G>T	XP_016867254.1:n.116+4052G>T
XM_017011766.2:c.116+4052G>T	XP_016867255.1:n.116+4052G>T
XM_024446669.1:c.98+4052G>T	XP_024302437.1:n.98+4052G>T
NM_001134405.2:c.458+4052G>T MANE Select	NP_001127877.1:n.458+4052G>T
NM_001134406.2:c.458+4052G>T	NP_001127878.1:n.458+4052G>T
NM_138290.3:c.509+4052G>T	NP_612147.1:n.509+4052G>T
NM_001394224.1:c.509+4052G>T	NP_001381153.1:n.509+4052G>T
NM_001394225.1:c.458+4052G>T	NP_001381154.1:n.458+4052G>T
NM_001394226.1:c.458+4052G>T	NP_001381155.1:n.458+4052G>T
NM_001394227.1:c.509+4052G>T	NP_001381156.1:n.509+4052G>T
NM_001394228.1:c.116+4052G>T	NP_001381157.1:n.116+4052G>T