Canonical Allele Identifier: CA2270103043

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832179C= , CM000679.2:g.63832179C=	GRCh38
NC_000017.10:g.61909539C= , CM000679.1:g.61909539C=	GRCh37
NC_000017.9:g.59263271C=	NCBI36
NG_053004.1:g.15813G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2634G=
ENST00000697953.1:n.3207G=
ENST00000698013.1:n.3319G=
ENST00000698014.1:n.3542G=
ENST00000698015.1:n.2635G=
ENST00000698016.1:c.*759G=	ENSP00000513502.1:n.*759G=
ENST00000698017.1:n.2709G=
ENST00000698018.1:n.2840G=
ENST00000698019.1:n.3038G=
ENST00000698020.1:n.2144G=
ENST00000698021.1:c.2053G=
ENST00000698022.1:c.*759G=	ENSP00000513504.1:n.*759G=
ENST00000698023.1:n.2738G=
ENST00000698024.1:n.2600G=
ENST00000698025.1:n.2760G=
ENST00000698026.1:n.1651G=
ENST00000698027.1:c.*976G=	ENSP00000513505.1:n.*976G=
ENST00000448276.7:c.*759G= MANE Select	ENSP00000392617.2:n.*759G=
ENST00000448276.6:c.*759G=	ENSP00000392617.2:n.*759G=
ENST00000613943.4:c.2244G=	ENSP00000483605.1:n.2244G=
NM_001098426.1:c.*759G=	NP_001091896.1:n.*759G=
XM_005257604.2:c.*759G=	XP_005257661.2:n.*759G=
NM_001330439.1:c.*759G=	NP_001317368.1:n.*759G=
NM_001330440.1:c.*759G=	NP_001317369.1:n.*759G=
NM_001098426.2:c.*759G= MANE Select	NP_001091896.1:n.*759G=
NM_001330440.2:c.*759G=	NP_001317369.1:n.*759G=