Canonical Allele Identifier: CA2397981344

Gene: DERL3 SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23834517C= , CM000684.2:g.23834517C=	GRCh38
NC_000022.10:g.24176704C= , CM000684.1:g.24176704C=	GRCh37
NC_000022.9:g.22506704C=	NCBI36
NG_009303.1:g.52555C= , LRG_520:g.52555C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318109.12:c.*2352G= (DERL3) MANE Select	ENSP00000315303.8:n.*2352G=
ENST00000407422.8:c.*337C= (SMARCB1)	ENSP00000383984.3:n.*337C=
ENST00000644036.2:c.*337C= (SMARCB1) MANE Select	ENSP00000494049.2:n.*337C=
ENST00000290730.11:n.3511G= (DERL3)
ENST00000404056.1:c.*2543G= (DERL3)	ENSP00000384473.1:n.*2543G=
ENST00000406855.7:c.*310G= (DERL3)	ENSP00000384744.3:n.*310G=
ENST00000464023.1:n.631G= (DERL3)
NM_001002862.2:c.*2352G= (DERL3)	NP_001002862.1:n.*2352G=
NM_001007468.1:c.*337C= (SMARCB1)	NP_001007469.1:n.*337C=
NM_001135751.1:c.*310G= (DERL3)	NP_001129223.1:n.*310G=
NM_003073.3:c.*337C= , LRG_520t1:c.*337C= (SMARCB1)	NP_003064.2:n.*337C=
NM_198440.3:c.*2543G= (DERL3)	NP_940842.2:n.*2543G=
XM_011530504.1:c.*310G= (DERL3)	XP_011528806.1:n.*310G=
XM_011530506.1:c.*375G= (DERL3)	XP_011528808.1:n.*375G=
XM_011530507.1:c.*310G= (DERL3)	XP_011528809.1:n.*310G=
NM_001007468.2:c.*337C= (SMARCB1)	NP_001007469.1:n.*337C=
NM_001317946.1:c.*337C= (SMARCB1)	NP_001304875.1:n.*337C=
NM_001362877.1:c.*337C= (SMARCB1)	NP_001349806.1:n.*337C=
NM_001363072.1:c.*375G= (DERL3)	NP_001350001.1:n.*375G=
NM_003073.4:c.*337C= (SMARCB1)	NP_003064.2:n.*337C=
XM_017029082.2:c.*310G= (DERL3)	XP_016884571.1:n.*310G=
NM_001002862.3:c.*2352G= (DERL3) MANE Select	NP_001002862.1:n.*2352G=
NM_001007468.3:c.*337C= (SMARCB1)	NP_001007469.1:n.*337C=
NM_001135751.2:c.*310G= (DERL3)	NP_001129223.1:n.*310G=
NM_001317946.2:c.*337C= (SMARCB1)	NP_001304875.1:n.*337C=
NM_001362877.2:c.*337C= (SMARCB1)	NP_001349806.1:n.*337C=
NM_001363072.2:c.*375G= (DERL3)	NP_001350001.1:n.*375G=
NM_003073.5:c.*337C= (SMARCB1) MANE Select	NP_003064.2:n.*337C=
NM_198440.4:c.*2543G= (DERL3)	NP_940842.2:n.*2543G=