Canonical Allele Identifier: CA2655715746

Gene: DERL3 SMARCB1

Linked Data

• gnomAD v4: 22-23834544-T-TCTTCAACAGGTCATGTTCAATTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.23834544_23834545insCTTCAACAGGTCATGTTCAATTTC , CM000684.2:g.23834544_23834545insCTTCAACAGGTCATGTTCAATTTC	GRCh38
NC_000022.10:g.24176731_24176732insCTTCAACAGGTCATGTTCAATTTC , CM000684.1:g.24176731_24176732insCTTCAACAGGTCATGTTCAATTTC	GRCh37
NC_000022.9:g.22506731_22506732insCTTCAACAGGTCATGTTCAATTTC	NCBI36
NG_009303.1:g.52582_52583insCTTCAACAGGTCATGTTCAATTTC , LRG_520:g.52582_52583insCTTCAACAGGTCATGTTCAATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318109.12:c.*2324_*2325insGAAATTGAACATGACCTGTTGAAG (DERL3) MANE Select	ENSP00000315303.8:n.*2324_*2325insGAAATTGAACATGACCTGTTGAAG
ENST00000644036.2:c.*364_*365insCTTCAACAGGTCATGTTCAATTTC (SMARCB1) MANE Select	ENSP00000494049.2:n.*364_*365insCTTCAACAGGTCATGTTCAATTTC
ENST00000290730.11:n.3483_3484insGAAATTGAACATGACCTGTTGAAG (DERL3)
ENST00000404056.1:c.*2515_*2516insGAAATTGAACATGACCTGTTGAAG (DERL3)	ENSP00000384473.1:n.*2515_*2516insGAAATTGAACATGACCTGTTGAAG
ENST00000406855.7:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	ENSP00000384744.3:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
ENST00000464023.1:n.603_604insGAAATTGAACATGACCTGTTGAAG (DERL3)
NM_001002862.2:c.*2324_*2325insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_001002862.1:n.*2324_*2325insGAAATTGAACATGACCTGTTGAAG
NM_001135751.1:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_001129223.1:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
NM_198440.3:c.*2515_*2516insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_940842.2:n.*2515_*2516insGAAATTGAACATGACCTGTTGAAG
XM_011530504.1:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	XP_011528806.1:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
XM_011530506.1:c.*347_*348insGAAATTGAACATGACCTGTTGAAG (DERL3)	XP_011528808.1:n.*347_*348insGAAATTGAACATGACCTGTTGAAG
XM_011530507.1:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	XP_011528809.1:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
NM_001363072.1:c.*347_*348insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_001350001.1:n.*347_*348insGAAATTGAACATGACCTGTTGAAG
XM_017029082.2:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	XP_016884571.1:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
NM_001002862.3:c.*2324_*2325insGAAATTGAACATGACCTGTTGAAG (DERL3) MANE Select	NP_001002862.1:n.*2324_*2325insGAAATTGAACATGACCTGTTGAAG
NM_001007468.3:c.*364_*365insCTTCAACAGGTCATGTTCAATTTC (SMARCB1)	NP_001007469.1:n.*364_*365insCTTCAACAGGTCATGTTCAATTTC
NM_001135751.2:c.*282_*283insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_001129223.1:n.*282_*283insGAAATTGAACATGACCTGTTGAAG
NM_001317946.2:c.*364_*365insCTTCAACAGGTCATGTTCAATTTC (SMARCB1)	NP_001304875.1:n.*364_*365insCTTCAACAGGTCATGTTCAATTTC
NM_001362877.2:c.*364_*365insCTTCAACAGGTCATGTTCAATTTC (SMARCB1)	NP_001349806.1:n.*364_*365insCTTCAACAGGTCATGTTCAATTTC
NM_001363072.2:c.*347_*348insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_001350001.1:n.*347_*348insGAAATTGAACATGACCTGTTGAAG
NM_003073.5:c.*364_*365insCTTCAACAGGTCATGTTCAATTTC (SMARCB1) MANE Select	NP_003064.2:n.*364_*365insCTTCAACAGGTCATGTTCAATTTC
NM_198440.4:c.*2515_*2516insGAAATTGAACATGACCTGTTGAAG (DERL3)	NP_940842.2:n.*2515_*2516insGAAATTGAACATGACCTGTTGAAG