Canonical Allele Identifier: CA827683271

Gene: RREB1

Linked Data

• dbSNP Id: rs11755724
• MyVariant Identifiers: chr6:g.7118990A>T (hg19) ; chr6:g.7118757A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.7118757A>T , CM000668.2:g.7118757A>T	GRCh38
NC_000006.11:g.7118990A>T , CM000668.1:g.7118990A>T	GRCh37
NC_000006.10:g.7063989A>T	NCBI36
NG_016201.1:g.16161A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000379938.7:c.-285+10697A>T MANE Select	ENSP00000369270.2:n.-285+10697A>T
ENST00000334984.10:c.-285+10697A>T	ENSP00000335574.6:n.-285+10697A>T
ENST00000349384.10:c.-285+10697A>T	ENSP00000305560.10:n.-285+10697A>T
ENST00000379933.7:c.-285+10989A>T	ENSP00000369265.3:n.-285+10989A>T
ENST00000379938.6:c.-285+10697A>T	ENSP00000369270.2:n.-285+10697A>T
ENST00000467782.5:c.-197+10697A>T	ENSP00000420571.1:n.-197+10697A>T
ENST00000471433.5:c.-285+10693A>T	ENSP00000420299.1:n.-285+10693A>T
ENST00000475946.5:n.71+10055A>T
ENST00000491191.5:c.-328+10697A>T	ENSP00000420519.1:n.-328+10697A>T
NM_001003698.3:c.-285+10697A>T	NP_001003698.1:n.-285+10697A>T
NM_001003699.3:c.-285+10697A>T	NP_001003699.1:n.-285+10697A>T
NM_001003700.1:c.-285+10697A>T	NP_001003700.1:n.-285+10697A>T
NM_001168344.1:c.-285+10989A>T	NP_001161816.1:n.-285+10989A>T
XM_005249275.2:c.-285+10055A>T	XP_005249332.1:n.-285+10055A>T
XM_011514792.1:c.-285+10693A>T	XP_011513094.1:n.-285+10693A>T
XM_011514793.1:c.-285+10989A>T	XP_011513095.1:n.-285+10989A>T
XM_011514794.1:c.-237+10697A>T	XP_011513096.1:n.-237+10697A>T
XM_011514795.1:c.-285+10697A>T	XP_011513097.1:n.-285+10697A>T
NM_001003699.4:c.-285+10697A>T MANE Select	NP_001003699.1:n.-285+10697A>T
NM_001003698.4:c.-285+10697A>T	NP_001003698.1:n.-285+10697A>T
NM_001003700.2:c.-285+10697A>T	NP_001003700.1:n.-285+10697A>T
NM_001168344.2:c.-285+10989A>T	NP_001161816.1:n.-285+10989A>T