Canonical Allele Identifier: CA2270103193

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832232_63832233delinsAC , CM000679.2:g.63832232_63832233delinsAC	GRCh38
NC_000017.10:g.61909592_61909593delinsAC , CM000679.1:g.61909592_61909593delinsAC	GRCh37
NC_000017.9:g.59263324_59263325delinsAC	NCBI36
NG_053004.1:g.15759_15760delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2580_2581delinsGT
ENST00000697953.1:n.3153_3154delinsGT
ENST00000698013.1:n.3265_3266delinsGT
ENST00000698014.1:n.3488_3489delinsGT
ENST00000698015.1:n.2581_2582delinsGT
ENST00000698016.1:c.*705_*706delinsGT	ENSP00000513502.1:n.*705_*706delinsGT
ENST00000698017.1:n.2655_2656delinsGT
ENST00000698018.1:n.2786_2787delinsGT
ENST00000698019.1:n.2984_2985delinsGT
ENST00000698020.1:n.2090_2091delinsGT
ENST00000698021.1:c.1999_2000delinsGT
ENST00000698022.1:c.*705_*706delinsGT	ENSP00000513504.1:n.*705_*706delinsGT
ENST00000698023.1:n.2684_2685delinsGT
ENST00000698024.1:n.2546_2547delinsGT
ENST00000698025.1:n.2706_2707delinsGT
ENST00000698026.1:n.1597_1598delinsGT
ENST00000698027.1:c.*922_*923delinsGT	ENSP00000513505.1:n.*922_*923delinsGT
ENST00000698028.1:n.2789_2790delinsGT
ENST00000448276.7:c.*705_*706delinsGT MANE Select	ENSP00000392617.2:n.*705_*706delinsGT
ENST00000448276.6:c.*705_*706delinsGT	ENSP00000392617.2:n.*705_*706delinsGT
ENST00000613943.4:c.2190_2191delinsGT	ENSP00000483605.1:n.2190_2191delinsGT
NM_001098426.1:c.*705_*706delinsGT	NP_001091896.1:n.*705_*706delinsGT
XM_005257604.2:c.*705_*706delinsGT	XP_005257661.2:n.*705_*706delinsGT
NM_001330439.1:c.*705_*706delinsGT	NP_001317368.1:n.*705_*706delinsGT
NM_001330440.1:c.*705_*706delinsGT	NP_001317369.1:n.*705_*706delinsGT
NM_001098426.2:c.*705_*706delinsGT MANE Select	NP_001091896.1:n.*705_*706delinsGT
NM_001330440.2:c.*705_*706delinsGT	NP_001317369.1:n.*705_*706delinsGT