Canonical Allele Identifier: CA2270103030

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832152C= , CM000679.2:g.63832152C=	GRCh38
NC_000017.10:g.61909512C= , CM000679.1:g.61909512C=	GRCh37
NC_000017.9:g.59263244C=	NCBI36
NG_053004.1:g.15840G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2661G=
ENST00000697953.1:n.3234G=
ENST00000698013.1:n.3346G=
ENST00000698014.1:n.3569G=
ENST00000698015.1:n.2662G=
ENST00000698016.1:c.*786G=	ENSP00000513502.1:n.*786G=
ENST00000698017.1:n.2736G=
ENST00000698018.1:n.2867G=
ENST00000698019.1:n.3065G=
ENST00000698020.1:n.2171G=
ENST00000698021.1:c.2080G=
ENST00000698022.1:c.*786G=	ENSP00000513504.1:n.*786G=
ENST00000698023.1:n.2765G=
ENST00000698024.1:n.2627G=
ENST00000698025.1:n.2787G=
ENST00000698026.1:n.1678G=
ENST00000698027.1:c.*1003G=	ENSP00000513505.1:n.*1003G=
ENST00000448276.7:c.*786G= MANE Select	ENSP00000392617.2:n.*786G=
ENST00000448276.6:c.*786G=	ENSP00000392617.2:n.*786G=
ENST00000613943.4:c.2271G=	ENSP00000483605.1:n.2271G=
NM_001098426.1:c.*786G=	NP_001091896.1:n.*786G=
XM_005257604.2:c.*786G=	XP_005257661.2:n.*786G=
NM_001330439.1:c.*786G=	NP_001317368.1:n.*786G=
NM_001330440.1:c.*786G=	NP_001317369.1:n.*786G=
NM_001098426.2:c.*786G= MANE Select	NP_001091896.1:n.*786G=
NM_001330440.2:c.*786G=	NP_001317369.1:n.*786G=