Canonical Allele Identifier: CA2270103122

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832552T= , CM000679.2:g.63832552T=	GRCh38
NC_000017.10:g.61909912T= , CM000679.1:g.61909912T=	GRCh37
NC_000017.9:g.59263644T=	NCBI36
NG_053004.1:g.15440A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2261A=
ENST00000697953.1:n.2834A=
ENST00000698013.1:n.2946A=
ENST00000698014.1:n.3169A=
ENST00000698015.1:n.2262A=
ENST00000698016.1:c.*386A=	ENSP00000513502.1:n.*386A=
ENST00000698017.1:n.2336A=
ENST00000698018.1:n.2467A=
ENST00000698019.1:n.2665A=
ENST00000698020.1:n.1771A=
ENST00000698021.1:c.1680A=
ENST00000698022.1:c.*386A=	ENSP00000513504.1:n.*386A=
ENST00000698023.1:n.2365A=
ENST00000698024.1:n.2227A=
ENST00000698025.1:n.2387A=
ENST00000698026.1:n.1278A=
ENST00000698027.1:c.*603A=	ENSP00000513505.1:n.*603A=
ENST00000698028.1:n.2470A=
ENST00000698029.1:n.3199A=
ENST00000448276.7:c.*386A= MANE Select	ENSP00000392617.2:n.*386A=
ENST00000323347.14:c.*386A=	ENSP00000318451.10:n.*386A=
ENST00000448276.6:c.*386A=	ENSP00000392617.2:n.*386A=
ENST00000613943.4:c.1871A=	ENSP00000483605.1:n.1871A=
NM_001098426.1:c.*386A=	NP_001091896.1:n.*386A=
XM_005257604.2:c.*386A=	XP_005257661.2:n.*386A=
NM_001330439.1:c.*386A=	NP_001317368.1:n.*386A=
NM_001330440.1:c.*386A=	NP_001317369.1:n.*386A=
NM_001098426.2:c.*386A= MANE Select	NP_001091896.1:n.*386A=
NM_001330440.2:c.*386A=	NP_001317369.1:n.*386A=