Canonical Allele Identifier: CA2270103377

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832347G= , CM000679.2:g.63832347G=	GRCh38
NC_000017.10:g.61909707G= , CM000679.1:g.61909707G=	GRCh37
NC_000017.9:g.59263439G=	NCBI36
NG_053004.1:g.15645C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2466C=
ENST00000697953.1:n.3039C=
ENST00000698013.1:n.3151C=
ENST00000698014.1:n.3374C=
ENST00000698015.1:n.2467C=
ENST00000698016.1:c.*591C=	ENSP00000513502.1:n.*591C=
ENST00000698017.1:n.2541C=
ENST00000698018.1:n.2672C=
ENST00000698019.1:n.2870C=
ENST00000698020.1:n.1976C=
ENST00000698021.1:c.1885C=
ENST00000698022.1:c.*591C=	ENSP00000513504.1:n.*591C=
ENST00000698023.1:n.2570C=
ENST00000698024.1:n.2432C=
ENST00000698025.1:n.2592C=
ENST00000698026.1:n.1483C=
ENST00000698027.1:c.*808C=	ENSP00000513505.1:n.*808C=
ENST00000698028.1:n.2675C=
ENST00000698029.1:n.3404C=
ENST00000448276.7:c.*591C= MANE Select	ENSP00000392617.2:n.*591C=
ENST00000448276.6:c.*591C=	ENSP00000392617.2:n.*591C=
ENST00000613943.4:c.2076C=	ENSP00000483605.1:n.2076C=
NM_001098426.1:c.*591C=	NP_001091896.1:n.*591C=
XM_005257604.2:c.*591C=	XP_005257661.2:n.*591C=
NM_001330439.1:c.*591C=	NP_001317368.1:n.*591C=
NM_001330440.1:c.*591C=	NP_001317369.1:n.*591C=
NM_001098426.2:c.*591C= MANE Select	NP_001091896.1:n.*591C=
NM_001330440.2:c.*591C=	NP_001317369.1:n.*591C=