Canonical Allele Identifier: CA2270103402

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832364_63832367delinsAAGG , CM000679.2:g.63832364_63832367delinsAAGG	GRCh38
NC_000017.10:g.61909724_61909727delinsAAGG , CM000679.1:g.61909724_61909727delinsAAGG	GRCh37
NC_000017.9:g.59263456_59263459delinsAAGG	NCBI36
NG_053004.1:g.15625_15628delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2446_2449delinsCCTT
ENST00000697953.1:n.3019_3022delinsCCTT
ENST00000698013.1:n.3131_3134delinsCCTT
ENST00000698014.1:n.3354_3357delinsCCTT
ENST00000698015.1:n.2447_2450delinsCCTT
ENST00000698016.1:c.*571_*574delinsCCTT	ENSP00000513502.1:n.*571_*574delinsCCTT
ENST00000698017.1:n.2521_2524delinsCCTT
ENST00000698018.1:n.2652_2655delinsCCTT
ENST00000698019.1:n.2850_2853delinsCCTT
ENST00000698020.1:n.1956_1959delinsCCTT
ENST00000698021.1:c.1865_1868delinsCCTT
ENST00000698022.1:c.*571_*574delinsCCTT	ENSP00000513504.1:n.*571_*574delinsCCTT
ENST00000698023.1:n.2550_2553delinsCCTT
ENST00000698024.1:n.2412_2415delinsCCTT
ENST00000698025.1:n.2572_2575delinsCCTT
ENST00000698026.1:n.1463_1466delinsCCTT
ENST00000698027.1:c.*788_*791delinsCCTT	ENSP00000513505.1:n.*788_*791delinsCCTT
ENST00000698028.1:n.2655_2658delinsCCTT
ENST00000698029.1:n.3384_3387delinsCCTT
ENST00000448276.7:c.*571_*574delinsCCTT MANE Select	ENSP00000392617.2:n.*571_*574delinsCCTT
ENST00000448276.6:c.*571_*574delinsCCTT	ENSP00000392617.2:n.*571_*574delinsCCTT
ENST00000613943.4:c.2056_2059delinsCCTT	ENSP00000483605.1:n.2056_2059delinsCCTT
NM_001098426.1:c.*571_*574delinsCCTT	NP_001091896.1:n.*571_*574delinsCCTT
XM_005257604.2:c.*571_*574delinsCCTT	XP_005257661.2:n.*571_*574delinsCCTT
NM_001330439.1:c.*571_*574delinsCCTT	NP_001317368.1:n.*571_*574delinsCCTT
NM_001330440.1:c.*571_*574delinsCCTT	NP_001317369.1:n.*571_*574delinsCCTT
NM_001098426.2:c.*571_*574delinsCCTT MANE Select	NP_001091896.1:n.*571_*574delinsCCTT
NM_001330440.2:c.*571_*574delinsCCTT	NP_001317369.1:n.*571_*574delinsCCTT