Canonical Allele Identifier: CA2270103082

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832459A= , CM000679.2:g.63832459A=	GRCh38
NC_000017.10:g.61909819A= , CM000679.1:g.61909819A=	GRCh37
NC_000017.9:g.59263551A=	NCBI36
NG_053004.1:g.15533T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2354T=
ENST00000697953.1:n.2927T=
ENST00000698013.1:n.3039T=
ENST00000698014.1:n.3262T=
ENST00000698015.1:n.2355T=
ENST00000698016.1:c.*479T=	ENSP00000513502.1:n.*479T=
ENST00000698017.1:n.2429T=
ENST00000698018.1:n.2560T=
ENST00000698019.1:n.2758T=
ENST00000698020.1:n.1864T=
ENST00000698021.1:c.1773T=
ENST00000698022.1:c.*479T=	ENSP00000513504.1:n.*479T=
ENST00000698023.1:n.2458T=
ENST00000698024.1:n.2320T=
ENST00000698025.1:n.2480T=
ENST00000698026.1:n.1371T=
ENST00000698027.1:c.*696T=	ENSP00000513505.1:n.*696T=
ENST00000698028.1:n.2563T=
ENST00000698029.1:n.3292T=
ENST00000448276.7:c.*479T= MANE Select	ENSP00000392617.2:n.*479T=
ENST00000448276.6:c.*479T=	ENSP00000392617.2:n.*479T=
ENST00000613943.4:c.1964T=	ENSP00000483605.1:n.1964T=
NM_001098426.1:c.*479T=	NP_001091896.1:n.*479T=
XM_005257604.2:c.*479T=	XP_005257661.2:n.*479T=
NM_001330439.1:c.*479T=	NP_001317368.1:n.*479T=
NM_001330440.1:c.*479T=	NP_001317369.1:n.*479T=
NM_001098426.2:c.*479T= MANE Select	NP_001091896.1:n.*479T=
NM_001330440.2:c.*479T=	NP_001317369.1:n.*479T=