Canonical Allele Identifier: CA2270103350

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832324_63832327delinsTGGC , CM000679.2:g.63832324_63832327delinsTGGC	GRCh38
NC_000017.10:g.61909684_61909687delinsTGGC , CM000679.1:g.61909684_61909687delinsTGGC	GRCh37
NC_000017.9:g.59263416_59263419delinsTGGC	NCBI36
NG_053004.1:g.15665_15668delinsGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2486_2489delinsGCCA
ENST00000697953.1:n.3059_3062delinsGCCA
ENST00000698013.1:n.3171_3174delinsGCCA
ENST00000698014.1:n.3394_3397delinsGCCA
ENST00000698015.1:n.2487_2490delinsGCCA
ENST00000698016.1:c.*611_*614delinsGCCA	ENSP00000513502.1:n.*611_*614delinsGCCA
ENST00000698017.1:n.2561_2564delinsGCCA
ENST00000698018.1:n.2692_2695delinsGCCA
ENST00000698019.1:n.2890_2893delinsGCCA
ENST00000698020.1:n.1996_1999delinsGCCA
ENST00000698021.1:c.1905_1908delinsGCCA
ENST00000698022.1:c.*611_*614delinsGCCA	ENSP00000513504.1:n.*611_*614delinsGCCA
ENST00000698023.1:n.2590_2593delinsGCCA
ENST00000698024.1:n.2452_2455delinsGCCA
ENST00000698025.1:n.2612_2615delinsGCCA
ENST00000698026.1:n.1503_1506delinsGCCA
ENST00000698027.1:c.*828_*831delinsGCCA	ENSP00000513505.1:n.*828_*831delinsGCCA
ENST00000698028.1:n.2695_2698delinsGCCA
ENST00000698029.1:n.3424_3427delinsGCCA
ENST00000448276.7:c.*611_*614delinsGCCA MANE Select	ENSP00000392617.2:n.*611_*614delinsGCCA
ENST00000448276.6:c.*611_*614delinsGCCA	ENSP00000392617.2:n.*611_*614delinsGCCA
ENST00000613943.4:c.2096_2099delinsGCCA	ENSP00000483605.1:n.2096_2099delinsGCCA
NM_001098426.1:c.*611_*614delinsGCCA	NP_001091896.1:n.*611_*614delinsGCCA
XM_005257604.2:c.*611_*614delinsGCCA	XP_005257661.2:n.*611_*614delinsGCCA
NM_001330439.1:c.*611_*614delinsGCCA	NP_001317368.1:n.*611_*614delinsGCCA
NM_001330440.1:c.*611_*614delinsGCCA	NP_001317369.1:n.*611_*614delinsGCCA
NM_001098426.2:c.*611_*614delinsGCCA MANE Select	NP_001091896.1:n.*611_*614delinsGCCA
NM_001330440.2:c.*611_*614delinsGCCA	NP_001317369.1:n.*611_*614delinsGCCA