Canonical Allele Identifier: CA2397981362

Gene: DERL3 SMARCB1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23834563A= , CM000684.2:g.23834563A=	GRCh38
NC_000022.10:g.24176750A= , CM000684.1:g.24176750A=	GRCh37
NC_000022.9:g.22506750A=	NCBI36
NG_009303.1:g.52601A= , LRG_520:g.52601A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318109.12:c.*2306T= (DERL3) MANE Select	ENSP00000315303.8:n.*2306T=
ENST00000644036.2:c.*383A= (SMARCB1) MANE Select	ENSP00000494049.2:n.*383A=
ENST00000290730.11:n.3465T= (DERL3)
ENST00000404056.1:c.*2497T= (DERL3)	ENSP00000384473.1:n.*2497T=
ENST00000406855.7:c.*264T= (DERL3)	ENSP00000384744.3:n.*264T=
ENST00000464023.1:n.585T= (DERL3)
NM_001002862.2:c.*2306T= (DERL3)	NP_001002862.1:n.*2306T=
NM_001135751.1:c.*264T= (DERL3)	NP_001129223.1:n.*264T=
NM_198440.3:c.*2497T= (DERL3)	NP_940842.2:n.*2497T=
XM_011530504.1:c.*264T= (DERL3)	XP_011528806.1:n.*264T=
XM_011530506.1:c.*329T= (DERL3)	XP_011528808.1:n.*329T=
XM_011530507.1:c.*264T= (DERL3)	XP_011528809.1:n.*264T=
NM_001363072.1:c.*329T= (DERL3)	NP_001350001.1:n.*329T=
XM_017029082.2:c.*264T= (DERL3)	XP_016884571.1:n.*264T=
NM_001002862.3:c.*2306T= (DERL3) MANE Select	NP_001002862.1:n.*2306T=
NM_001007468.3:c.*383A= (SMARCB1)	NP_001007469.1:n.*383A=
NM_001135751.2:c.*264T= (DERL3)	NP_001129223.1:n.*264T=
NM_001317946.2:c.*383A= (SMARCB1)	NP_001304875.1:n.*383A=
NM_001362877.2:c.*383A= (SMARCB1)	NP_001349806.1:n.*383A=
NM_001363072.2:c.*329T= (DERL3)	NP_001350001.1:n.*329T=
NM_003073.5:c.*383A= (SMARCB1) MANE Select	NP_003064.2:n.*383A=
NM_198440.4:c.*2497T= (DERL3)	NP_940842.2:n.*2497T=