Canonical Allele Identifier: CA2270105445

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837239_63837240delinsTG , CM000679.2:g.63837239_63837240delinsTG	GRCh38
NC_000017.10:g.61914599_61914600delinsTG , CM000679.1:g.61914599_61914600delinsTG	GRCh37
NC_000017.9:g.59268331_59268332delinsTG	NCBI36
NG_053004.1:g.10752_10753delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.490_491delinsCA
ENST00000698015.1:n.36-3_36-2delinsCA
ENST00000698016.1:c.261-3_261-2delinsCA	ENSP00000513502.1:n.261-3_261-2delinsCA
ENST00000698020.1:n.188_189delinsCA
ENST00000698021.1:c.65-3_65-2delinsCA
ENST00000698022.1:c.219-3_219-2delinsCA	ENSP00000513504.1:n.219-3_219-2delinsCA
ENST00000698027.1:c.261-3_261-2delinsCA	ENSP00000513505.1:n.261-3_261-2delinsCA
ENST00000448276.7:c.402-3_402-2delinsCA MANE Select	ENSP00000392617.2:n.402-3_402-2delinsCA
ENST00000225742.13:c.177-3_177-2delinsCA	ENSP00000225742.9:n.177-3_177-2delinsCA
ENST00000323347.14:c.258-3_258-2delinsCA	ENSP00000318451.10:n.258-3_258-2delinsCA
ENST00000448276.6:c.402-3_402-2delinsCA	ENSP00000392617.2:n.402-3_402-2delinsCA
ENST00000577686.1:n.53-3_53-2delinsCA
ENST00000580054.1:c.186-3_186-2delinsCA	ENSP00000463793.1:n.186-3_186-2delinsCA
ENST00000584400.5:c.217-3_217-2delinsCA	ENSP00000464503.1:n.217-3_217-2delinsCA
ENST00000613943.4:c.291-3_291-2delinsCA	ENSP00000483605.1:n.291-3_291-2delinsCA
NM_001098426.1:c.402-3_402-2delinsCA	NP_001091896.1:n.402-3_402-2delinsCA
XM_005257604.2:c.177-3_177-2delinsCA	XP_005257661.2:n.177-3_177-2delinsCA
NM_001330439.1:c.177-3_177-2delinsCA	NP_001317368.1:n.177-3_177-2delinsCA
NM_001330440.1:c.258-3_258-2delinsCA	NP_001317369.1:n.258-3_258-2delinsCA
NM_001098426.2:c.402-3_402-2delinsCA MANE Select	NP_001091896.1:n.402-3_402-2delinsCA
NM_001330440.2:c.258-3_258-2delinsCA	NP_001317369.1:n.258-3_258-2delinsCA