Canonical Allele Identifier: CA2810124112

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832485G>T , CM000679.2:g.63832485G>T	GRCh38
NC_000017.10:g.61909845G>T , CM000679.1:g.61909845G>T	GRCh37
NC_000017.9:g.59263577G>T	NCBI36
NG_053004.1:g.15507C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2328C>A
ENST00000697953.1:n.2901C>A
ENST00000698013.1:n.3013C>A
ENST00000698014.1:n.3236C>A
ENST00000698015.1:n.2329C>A
ENST00000698016.1:c.*453C>A	ENSP00000513502.1:n.*453C>A
ENST00000698017.1:n.2403C>A
ENST00000698018.1:n.2534C>A
ENST00000698019.1:n.2732C>A
ENST00000698020.1:n.1838C>A
ENST00000698021.1:c.1747C>A
ENST00000698022.1:c.*453C>A	ENSP00000513504.1:n.*453C>A
ENST00000698023.1:n.2432C>A
ENST00000698024.1:n.2294C>A
ENST00000698025.1:n.2454C>A
ENST00000698026.1:n.1345C>A
ENST00000698027.1:c.*670C>A	ENSP00000513505.1:n.*670C>A
ENST00000698028.1:n.2537C>A
ENST00000698029.1:n.3266C>A
ENST00000448276.7:c.*453C>A MANE Select	ENSP00000392617.2:n.*453C>A
ENST00000448276.6:c.*453C>A	ENSP00000392617.2:n.*453C>A
ENST00000613943.4:c.1938C>A	ENSP00000483605.1:n.1938C>A
NM_001098426.1:c.*453C>A	NP_001091896.1:n.*453C>A
XM_005257604.2:c.*453C>A	XP_005257661.2:n.*453C>A
NM_001330439.1:c.*453C>A	NP_001317368.1:n.*453C>A
NM_001330440.1:c.*453C>A	NP_001317369.1:n.*453C>A
NM_001098426.2:c.*453C>A MANE Select	NP_001091896.1:n.*453C>A
NM_001330440.2:c.*453C>A	NP_001317369.1:n.*453C>A