Canonical Allele Identifier: CA2270103066

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832422G= , CM000679.2:g.63832422G=	GRCh38
NC_000017.10:g.61909782G= , CM000679.1:g.61909782G=	GRCh37
NC_000017.9:g.59263514G=	NCBI36
NG_053004.1:g.15570C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2391C=
ENST00000697953.1:n.2964C=
ENST00000698013.1:n.3076C=
ENST00000698014.1:n.3299C=
ENST00000698015.1:n.2392C=
ENST00000698016.1:c.*516C=	ENSP00000513502.1:n.*516C=
ENST00000698017.1:n.2466C=
ENST00000698018.1:n.2597C=
ENST00000698019.1:n.2795C=
ENST00000698020.1:n.1901C=
ENST00000698021.1:c.1810C=
ENST00000698022.1:c.*516C=	ENSP00000513504.1:n.*516C=
ENST00000698023.1:n.2495C=
ENST00000698024.1:n.2357C=
ENST00000698025.1:n.2517C=
ENST00000698026.1:n.1408C=
ENST00000698027.1:c.*733C=	ENSP00000513505.1:n.*733C=
ENST00000698028.1:n.2600C=
ENST00000698029.1:n.3329C=
ENST00000448276.7:c.*516C= MANE Select	ENSP00000392617.2:n.*516C=
ENST00000448276.6:c.*516C=	ENSP00000392617.2:n.*516C=
ENST00000613943.4:c.2001C=	ENSP00000483605.1:n.2001C=
NM_001098426.1:c.*516C=	NP_001091896.1:n.*516C=
XM_005257604.2:c.*516C=	XP_005257661.2:n.*516C=
NM_001330439.1:c.*516C=	NP_001317368.1:n.*516C=
NM_001330440.1:c.*516C=	NP_001317369.1:n.*516C=
NM_001098426.2:c.*516C= MANE Select	NP_001091896.1:n.*516C=
NM_001330440.2:c.*516C=	NP_001317369.1:n.*516C=