Canonical Allele Identifier: CA409824620

Gene: RBM11

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.14216190T>C , CM000683.2:g.14216190T>C	GRCh38
NC_000021.8:g.15588511T>C , CM000683.1:g.15588511T>C	GRCh37
NC_000021.7:g.14510382T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_144770.5:c.4T>C MANE Select	NP_658983.3:p.Phe2Leu
ENST00000400577.4:c.4T>C MANE Select	ENSP00000383421.3:p.Phe2Leu
NM_001320602.1:c.4T>C	NP_001307531.1:p.Phe2Leu
NM_001320602.2:c.4T>C	NP_001307531.1:p.Phe2Leu
NM_144770.3:c.4T>C	NP_658983.3:p.Phe2Leu
NM_144770.4:c.4T>C	NP_658983.3:p.Phe2Leu
NR_135308.1:n.61T>C
NR_135308.2:n.34T>C
NR_135309.1:n.61T>C
NR_135309.2:n.34T>C
NR_135310.1:n.61T>C
NR_135310.2:n.34T>C
NR_135311.1:n.61T>C
NR_135311.2:n.34T>C
ENST00000400577.3:c.4T>C	ENSP00000383421.3:p.Phe2Leu
ENST00000461088.1:n.37T>C
ENST00000468643.5:n.61T>C
ENST00000468788.5:n.46T>C
ENST00000495055.1:n.38T>C
XM_005260996.2:c.4T>C	XP_005261053.1:p.Phe2Leu
XM_005260997.3:c.4T>C	XP_005261054.1:p.Phe2Leu
XM_005260997.5:c.4T>C	XP_005261054.1:p.Phe2Leu
XM_005260998.2:c.-349T>C	XP_005261055.1:n.-349T>C
XM_006724017.2:c.4T>C	XP_006724080.1:p.Phe2Leu
XM_017028386.1:c.-498T>C	XP_016883875.1:n.-498T>C
XM_017028387.1:c.-488T>C	XP_016883876.1:n.-488T>C