Canonical Allele Identifier: CA2270103432

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832403_63832404delinsAC , CM000679.2:g.63832403_63832404delinsAC	GRCh38
NC_000017.10:g.61909763_61909764delinsAC , CM000679.1:g.61909763_61909764delinsAC	GRCh37
NC_000017.9:g.59263495_59263496delinsAC	NCBI36
NG_053004.1:g.15588_15589delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2409_2410delinsGT
ENST00000697953.1:n.2982_2983delinsGT
ENST00000698013.1:n.3094_3095delinsGT
ENST00000698014.1:n.3317_3318delinsGT
ENST00000698015.1:n.2410_2411delinsGT
ENST00000698016.1:c.*534_*535delinsGT	ENSP00000513502.1:n.*534_*535delinsGT
ENST00000698017.1:n.2484_2485delinsGT
ENST00000698018.1:n.2615_2616delinsGT
ENST00000698019.1:n.2813_2814delinsGT
ENST00000698020.1:n.1919_1920delinsGT
ENST00000698021.1:c.1828_1829delinsGT
ENST00000698022.1:c.*534_*535delinsGT	ENSP00000513504.1:n.*534_*535delinsGT
ENST00000698023.1:n.2513_2514delinsGT
ENST00000698024.1:n.2375_2376delinsGT
ENST00000698025.1:n.2535_2536delinsGT
ENST00000698026.1:n.1426_1427delinsGT
ENST00000698027.1:c.*751_*752delinsGT	ENSP00000513505.1:n.*751_*752delinsGT
ENST00000698028.1:n.2618_2619delinsGT
ENST00000698029.1:n.3347_3348delinsGT
ENST00000448276.7:c.*534_*535delinsGT MANE Select	ENSP00000392617.2:n.*534_*535delinsGT
ENST00000448276.6:c.*534_*535delinsGT	ENSP00000392617.2:n.*534_*535delinsGT
ENST00000613943.4:c.2019_2020delinsGT	ENSP00000483605.1:n.2019_2020delinsGT
NM_001098426.1:c.*534_*535delinsGT	NP_001091896.1:n.*534_*535delinsGT
XM_005257604.2:c.*534_*535delinsGT	XP_005257661.2:n.*534_*535delinsGT
NM_001330439.1:c.*534_*535delinsGT	NP_001317368.1:n.*534_*535delinsGT
NM_001330440.1:c.*534_*535delinsGT	NP_001317369.1:n.*534_*535delinsGT
NM_001098426.2:c.*534_*535delinsGT MANE Select	NP_001091896.1:n.*534_*535delinsGT
NM_001330440.2:c.*534_*535delinsGT	NP_001317369.1:n.*534_*535delinsGT