Canonical Allele Identifier: CA2270105487

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837326_63837327delinsTC , CM000679.2:g.63837326_63837327delinsTC	GRCh38
NC_000017.10:g.61914686_61914687delinsTC , CM000679.1:g.61914686_61914687delinsTC	GRCh37
NC_000017.9:g.59268418_59268419delinsTC	NCBI36
NG_053004.1:g.10665_10666delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.403_404delinsGA
ENST00000698015.1:n.36-90_36-89delinsGA
ENST00000698016.1:c.261-90_261-89delinsGA	ENSP00000513502.1:n.261-90_261-89delinsGA
ENST00000698020.1:n.101_102delinsGA
ENST00000698021.1:c.65-90_65-89delinsGA
ENST00000698022.1:c.219-90_219-89delinsGA	ENSP00000513504.1:n.219-90_219-89delinsGA
ENST00000698027.1:c.261-90_261-89delinsGA	ENSP00000513505.1:n.261-90_261-89delinsGA
ENST00000448276.7:c.402-90_402-89delinsGA MANE Select	ENSP00000392617.2:n.402-90_402-89delinsGA
ENST00000225742.13:c.177-90_177-89delinsGA	ENSP00000225742.9:n.177-90_177-89delinsGA
ENST00000323347.14:c.258-90_258-89delinsGA	ENSP00000318451.10:n.258-90_258-89delinsGA
ENST00000448276.6:c.402-90_402-89delinsGA	ENSP00000392617.2:n.402-90_402-89delinsGA
ENST00000577686.1:n.53-90_53-89delinsGA
ENST00000580054.1:c.186-90_186-89delinsGA	ENSP00000463793.1:n.186-90_186-89delinsGA
ENST00000584400.5:c.217-90_217-89delinsGA	ENSP00000464503.1:n.217-90_217-89delinsGA
ENST00000613943.4:c.291-90_291-89delinsGA	ENSP00000483605.1:n.291-90_291-89delinsGA
NM_001098426.1:c.402-90_402-89delinsGA	NP_001091896.1:n.402-90_402-89delinsGA
XM_005257604.2:c.177-90_177-89delinsGA	XP_005257661.2:n.177-90_177-89delinsGA
NM_001330439.1:c.177-90_177-89delinsGA	NP_001317368.1:n.177-90_177-89delinsGA
NM_001330440.1:c.258-90_258-89delinsGA	NP_001317369.1:n.258-90_258-89delinsGA
NM_001098426.2:c.402-90_402-89delinsGA MANE Select	NP_001091896.1:n.402-90_402-89delinsGA
NM_001330440.2:c.258-90_258-89delinsGA	NP_001317369.1:n.258-90_258-89delinsGA