Canonical Allele Identifier: CA2270103409

Gene: SMARCD2

Linked Data

• dbSNP Id: rs2040202727

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832372_63832382del , CM000679.2:g.63832372_63832382del	GRCh38
NC_000017.10:g.61909732_61909742del , CM000679.1:g.61909732_61909742del	GRCh37
NC_000017.9:g.59263464_59263474del	NCBI36
NG_053004.1:g.15614_15624del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2435_2445del
ENST00000697953.1:n.3008_3018del
ENST00000698013.1:n.3120_3130del
ENST00000698014.1:n.3343_3353del
ENST00000698015.1:n.2436_2446del
ENST00000698016.1:c.*560_*570del	ENSP00000513502.1:n.*560_*570del
ENST00000698017.1:n.2510_2520del
ENST00000698018.1:n.2641_2651del
ENST00000698019.1:n.2839_2849del
ENST00000698020.1:n.1945_1955del
ENST00000698021.1:c.1854_1864del
ENST00000698022.1:c.*560_*570del	ENSP00000513504.1:n.*560_*570del
ENST00000698023.1:n.2539_2549del
ENST00000698024.1:n.2401_2411del
ENST00000698025.1:n.2561_2571del
ENST00000698026.1:n.1452_1462del
ENST00000698027.1:c.*777_*787del	ENSP00000513505.1:n.*777_*787del
ENST00000698028.1:n.2644_2654del
ENST00000698029.1:n.3373_3383del
ENST00000448276.7:c.*560_*570del MANE Select	ENSP00000392617.2:n.*560_*570del
ENST00000448276.6:c.*560_*570del	ENSP00000392617.2:n.*560_*570del
ENST00000613943.4:c.2045_2055del	ENSP00000483605.1:n.2045_2055del
NM_001098426.1:c.*560_*570del	NP_001091896.1:n.*560_*570del
XM_005257604.2:c.*560_*570del	XP_005257661.2:n.*560_*570del
NM_001330439.1:c.*560_*570del	NP_001317368.1:n.*560_*570del
NM_001330440.1:c.*560_*570del	NP_001317369.1:n.*560_*570del
NM_001098426.2:c.*560_*570del MANE Select	NP_001091896.1:n.*560_*570del
NM_001330440.2:c.*560_*570del	NP_001317369.1:n.*560_*570del