Canonical Allele Identifier: CA2270103025

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832140G= , CM000679.2:g.63832140G=	GRCh38
NC_000017.10:g.61909500G= , CM000679.1:g.61909500G=	GRCh37
NC_000017.9:g.59263232G=	NCBI36
NG_053004.1:g.15852C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3246C=
ENST00000698013.1:n.3358C=
ENST00000698014.1:n.3581C=
ENST00000698015.1:n.2674C=
ENST00000698016.1:c.*798C=	ENSP00000513502.1:n.*798C=
ENST00000698017.1:n.2748C=
ENST00000698018.1:n.2879C=
ENST00000698019.1:n.3077C=
ENST00000698020.1:n.2183C=
ENST00000698021.1:c.2092C=
ENST00000698022.1:c.*798C=	ENSP00000513504.1:n.*798C=
ENST00000698023.1:n.2777C=
ENST00000698024.1:n.2639C=
ENST00000698025.1:n.2799C=
ENST00000698026.1:n.1690C=
ENST00000698027.1:c.*1015C=	ENSP00000513505.1:n.*1015C=
ENST00000448276.7:c.*798C= MANE Select	ENSP00000392617.2:n.*798C=
ENST00000448276.6:c.*798C=	ENSP00000392617.2:n.*798C=
ENST00000613943.4:c.2283C=	ENSP00000483605.1:n.2283C=
NM_001098426.1:c.*798C=	NP_001091896.1:n.*798C=
XM_005257604.2:c.*798C=	XP_005257661.2:n.*798C=
NM_001330439.1:c.*798C=	NP_001317368.1:n.*798C=
NM_001330440.1:c.*798C=	NP_001317369.1:n.*798C=
NM_001098426.2:c.*798C= MANE Select	NP_001091896.1:n.*798C=
NM_001330440.2:c.*798C=	NP_001317369.1:n.*798C=