Canonical Allele Identifier: CA2270103385

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832352A= , CM000679.2:g.63832352A=	GRCh38
NC_000017.10:g.61909712A= , CM000679.1:g.61909712A=	GRCh37
NC_000017.9:g.59263444A=	NCBI36
NG_053004.1:g.15640T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2461T=
ENST00000697953.1:n.3034T=
ENST00000698013.1:n.3146T=
ENST00000698014.1:n.3369T=
ENST00000698015.1:n.2462T=
ENST00000698016.1:c.*586T=	ENSP00000513502.1:n.*586T=
ENST00000698017.1:n.2536T=
ENST00000698018.1:n.2667T=
ENST00000698019.1:n.2865T=
ENST00000698020.1:n.1971T=
ENST00000698021.1:c.1880T=
ENST00000698022.1:c.*586T=	ENSP00000513504.1:n.*586T=
ENST00000698023.1:n.2565T=
ENST00000698024.1:n.2427T=
ENST00000698025.1:n.2587T=
ENST00000698026.1:n.1478T=
ENST00000698027.1:c.*803T=	ENSP00000513505.1:n.*803T=
ENST00000698028.1:n.2670T=
ENST00000698029.1:n.3399T=
ENST00000448276.7:c.*586T= MANE Select	ENSP00000392617.2:n.*586T=
ENST00000448276.6:c.*586T=	ENSP00000392617.2:n.*586T=
ENST00000613943.4:c.2071T=	ENSP00000483605.1:n.2071T=
NM_001098426.1:c.*586T=	NP_001091896.1:n.*586T=
XM_005257604.2:c.*586T=	XP_005257661.2:n.*586T=
NM_001330439.1:c.*586T=	NP_001317368.1:n.*586T=
NM_001330440.1:c.*586T=	NP_001317369.1:n.*586T=
NM_001098426.2:c.*586T= MANE Select	NP_001091896.1:n.*586T=
NM_001330440.2:c.*586T=	NP_001317369.1:n.*586T=