Canonical Allele Identifier: CA2810124105

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832306T>C , CM000679.2:g.63832306T>C	GRCh38
NC_000017.10:g.61909666T>C , CM000679.1:g.61909666T>C	GRCh37
NC_000017.9:g.59263398T>C	NCBI36
NG_053004.1:g.15686A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2507A>G
ENST00000697953.1:n.3080A>G
ENST00000698013.1:n.3192A>G
ENST00000698014.1:n.3415A>G
ENST00000698015.1:n.2508A>G
ENST00000698016.1:c.*632A>G	ENSP00000513502.1:n.*632A>G
ENST00000698017.1:n.2582A>G
ENST00000698018.1:n.2713A>G
ENST00000698019.1:n.2911A>G
ENST00000698020.1:n.2017A>G
ENST00000698021.1:c.1926A>G
ENST00000698022.1:c.*632A>G	ENSP00000513504.1:n.*632A>G
ENST00000698023.1:n.2611A>G
ENST00000698024.1:n.2473A>G
ENST00000698025.1:n.2633A>G
ENST00000698026.1:n.1524A>G
ENST00000698027.1:c.*849A>G	ENSP00000513505.1:n.*849A>G
ENST00000698028.1:n.2716A>G
ENST00000698029.1:n.3445A>G
ENST00000448276.7:c.*632A>G MANE Select	ENSP00000392617.2:n.*632A>G
ENST00000448276.6:c.*632A>G	ENSP00000392617.2:n.*632A>G
ENST00000613943.4:c.2117A>G	ENSP00000483605.1:n.2117A>G
NM_001098426.1:c.*632A>G	NP_001091896.1:n.*632A>G
XM_005257604.2:c.*632A>G	XP_005257661.2:n.*632A>G
NM_001330439.1:c.*632A>G	NP_001317368.1:n.*632A>G
NM_001330440.1:c.*632A>G	NP_001317369.1:n.*632A>G
NM_001098426.2:c.*632A>G MANE Select	NP_001091896.1:n.*632A>G
NM_001330440.2:c.*632A>G	NP_001317369.1:n.*632A>G