Canonical Allele Identifier: CA2270103363

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832333G= , CM000679.2:g.63832333G=	GRCh38
NC_000017.10:g.61909693G= , CM000679.1:g.61909693G=	GRCh37
NC_000017.9:g.59263425G=	NCBI36
NG_053004.1:g.15659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2480C=
ENST00000697953.1:n.3053C=
ENST00000698013.1:n.3165C=
ENST00000698014.1:n.3388C=
ENST00000698015.1:n.2481C=
ENST00000698016.1:c.*605C=	ENSP00000513502.1:n.*605C=
ENST00000698017.1:n.2555C=
ENST00000698018.1:n.2686C=
ENST00000698019.1:n.2884C=
ENST00000698020.1:n.1990C=
ENST00000698021.1:c.1899C=
ENST00000698022.1:c.*605C=	ENSP00000513504.1:n.*605C=
ENST00000698023.1:n.2584C=
ENST00000698024.1:n.2446C=
ENST00000698025.1:n.2606C=
ENST00000698026.1:n.1497C=
ENST00000698027.1:c.*822C=	ENSP00000513505.1:n.*822C=
ENST00000698028.1:n.2689C=
ENST00000698029.1:n.3418C=
ENST00000448276.7:c.*605C= MANE Select	ENSP00000392617.2:n.*605C=
ENST00000448276.6:c.*605C=	ENSP00000392617.2:n.*605C=
ENST00000613943.4:c.2090C=	ENSP00000483605.1:n.2090C=
NM_001098426.1:c.*605C=	NP_001091896.1:n.*605C=
XM_005257604.2:c.*605C=	XP_005257661.2:n.*605C=
NM_001330439.1:c.*605C=	NP_001317368.1:n.*605C=
NM_001330440.1:c.*605C=	NP_001317369.1:n.*605C=
NM_001098426.2:c.*605C= MANE Select	NP_001091896.1:n.*605C=
NM_001330440.2:c.*605C=	NP_001317369.1:n.*605C=