Canonical Allele Identifier: CA2270103399

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832360_63832363delinsAAAG , CM000679.2:g.63832360_63832363delinsAAAG	GRCh38
NC_000017.10:g.61909720_61909723delinsAAAG , CM000679.1:g.61909720_61909723delinsAAAG	GRCh37
NC_000017.9:g.59263452_59263455delinsAAAG	NCBI36
NG_053004.1:g.15629_15632delinsCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2450_2453delinsCTTT
ENST00000697953.1:n.3023_3026delinsCTTT
ENST00000698013.1:n.3135_3138delinsCTTT
ENST00000698014.1:n.3358_3361delinsCTTT
ENST00000698015.1:n.2451_2454delinsCTTT
ENST00000698016.1:c.*575_*578delinsCTTT	ENSP00000513502.1:n.*575_*578delinsCTTT
ENST00000698017.1:n.2525_2528delinsCTTT
ENST00000698018.1:n.2656_2659delinsCTTT
ENST00000698019.1:n.2854_2857delinsCTTT
ENST00000698020.1:n.1960_1963delinsCTTT
ENST00000698021.1:c.1869_1872delinsCTTT
ENST00000698022.1:c.*575_*578delinsCTTT	ENSP00000513504.1:n.*575_*578delinsCTTT
ENST00000698023.1:n.2554_2557delinsCTTT
ENST00000698024.1:n.2416_2419delinsCTTT
ENST00000698025.1:n.2576_2579delinsCTTT
ENST00000698026.1:n.1467_1470delinsCTTT
ENST00000698027.1:c.*792_*795delinsCTTT	ENSP00000513505.1:n.*792_*795delinsCTTT
ENST00000698028.1:n.2659_2662delinsCTTT
ENST00000698029.1:n.3388_3391delinsCTTT
ENST00000448276.7:c.*575_*578delinsCTTT MANE Select	ENSP00000392617.2:n.*575_*578delinsCTTT
ENST00000448276.6:c.*575_*578delinsCTTT	ENSP00000392617.2:n.*575_*578delinsCTTT
ENST00000613943.4:c.2060_2063delinsCTTT	ENSP00000483605.1:n.2060_2063delinsCTTT
NM_001098426.1:c.*575_*578delinsCTTT	NP_001091896.1:n.*575_*578delinsCTTT
XM_005257604.2:c.*575_*578delinsCTTT	XP_005257661.2:n.*575_*578delinsCTTT
NM_001330439.1:c.*575_*578delinsCTTT	NP_001317368.1:n.*575_*578delinsCTTT
NM_001330440.1:c.*575_*578delinsCTTT	NP_001317369.1:n.*575_*578delinsCTTT
NM_001098426.2:c.*575_*578delinsCTTT MANE Select	NP_001091896.1:n.*575_*578delinsCTTT
NM_001330440.2:c.*575_*578delinsCTTT	NP_001317369.1:n.*575_*578delinsCTTT