Canonical Allele Identifier: CA2270103063

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832412C= , CM000679.2:g.63832412C=	GRCh38
NC_000017.10:g.61909772C= , CM000679.1:g.61909772C=	GRCh37
NC_000017.9:g.59263504C=	NCBI36
NG_053004.1:g.15580G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2401G=
ENST00000697953.1:n.2974G=
ENST00000698013.1:n.3086G=
ENST00000698014.1:n.3309G=
ENST00000698015.1:n.2402G=
ENST00000698016.1:c.*526G=	ENSP00000513502.1:n.*526G=
ENST00000698017.1:n.2476G=
ENST00000698018.1:n.2607G=
ENST00000698019.1:n.2805G=
ENST00000698020.1:n.1911G=
ENST00000698021.1:c.1820G=
ENST00000698022.1:c.*526G=	ENSP00000513504.1:n.*526G=
ENST00000698023.1:n.2505G=
ENST00000698024.1:n.2367G=
ENST00000698025.1:n.2527G=
ENST00000698026.1:n.1418G=
ENST00000698027.1:c.*743G=	ENSP00000513505.1:n.*743G=
ENST00000698028.1:n.2610G=
ENST00000698029.1:n.3339G=
ENST00000448276.7:c.*526G= MANE Select	ENSP00000392617.2:n.*526G=
ENST00000448276.6:c.*526G=	ENSP00000392617.2:n.*526G=
ENST00000613943.4:c.2011G=	ENSP00000483605.1:n.2011G=
NM_001098426.1:c.*526G=	NP_001091896.1:n.*526G=
XM_005257604.2:c.*526G=	XP_005257661.2:n.*526G=
NM_001330439.1:c.*526G=	NP_001317368.1:n.*526G=
NM_001330440.1:c.*526G=	NP_001317369.1:n.*526G=
NM_001098426.2:c.*526G= MANE Select	NP_001091896.1:n.*526G=
NM_001330440.2:c.*526G=	NP_001317369.1:n.*526G=