Canonical Allele Identifier: CA2810124241

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837331_63837332del , CM000679.2:g.63837331_63837332del	GRCh38
NC_000017.10:g.61914691_61914692del , CM000679.1:g.61914691_61914692del	GRCh37
NC_000017.9:g.59268423_59268424del	NCBI36
NG_053004.1:g.10660_10661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.398_399del
ENST00000698015.1:n.36-95_36-94del
ENST00000698016.1:c.261-95_261-94del	ENSP00000513502.1:n.261-95_261-94del
ENST00000698020.1:n.96_97del
ENST00000698021.1:c.65-95_65-94del
ENST00000698022.1:c.219-95_219-94del	ENSP00000513504.1:n.219-95_219-94del
ENST00000698027.1:c.261-95_261-94del	ENSP00000513505.1:n.261-95_261-94del
ENST00000448276.7:c.402-95_402-94del MANE Select	ENSP00000392617.2:n.402-95_402-94del
ENST00000225742.13:c.177-95_177-94del	ENSP00000225742.9:n.177-95_177-94del
ENST00000323347.14:c.258-95_258-94del	ENSP00000318451.10:n.258-95_258-94del
ENST00000448276.6:c.402-95_402-94del	ENSP00000392617.2:n.402-95_402-94del
ENST00000577686.1:n.53-95_53-94del
ENST00000580054.1:c.186-95_186-94del	ENSP00000463793.1:n.186-95_186-94del
ENST00000584400.5:c.217-95_217-94del	ENSP00000464503.1:n.217-95_217-94del
ENST00000613943.4:c.291-95_291-94del	ENSP00000483605.1:n.291-95_291-94del
NM_001098426.1:c.402-95_402-94del	NP_001091896.1:n.402-95_402-94del
XM_005257604.2:c.177-95_177-94del	XP_005257661.2:n.177-95_177-94del
NM_001330439.1:c.177-95_177-94del	NP_001317368.1:n.177-95_177-94del
NM_001330440.1:c.258-95_258-94del	NP_001317369.1:n.258-95_258-94del
NM_001098426.2:c.402-95_402-94del MANE Select	NP_001091896.1:n.402-95_402-94del
NM_001330440.2:c.258-95_258-94del	NP_001317369.1:n.258-95_258-94del