Canonical Allele Identifier: CA2270103016

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832125T= , CM000679.2:g.63832125T=	GRCh38
NC_000017.10:g.61909485T= , CM000679.1:g.61909485T=	GRCh37
NC_000017.9:g.59263217T=	NCBI36
NG_053004.1:g.15867A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3261A=
ENST00000698013.1:n.3373A=
ENST00000698014.1:n.3596A=
ENST00000698015.1:n.2689A=
ENST00000698016.1:c.*813A=	ENSP00000513502.1:n.*813A=
ENST00000698017.1:n.2763A=
ENST00000698018.1:n.2894A=
ENST00000698019.1:n.3092A=
ENST00000698020.1:n.2198A=
ENST00000698021.1:c.2107A=
ENST00000698022.1:c.*813A=	ENSP00000513504.1:n.*813A=
ENST00000698023.1:n.2792A=
ENST00000698024.1:n.2654A=
ENST00000448276.7:c.*813A= MANE Select	ENSP00000392617.2:n.*813A=
ENST00000448276.6:c.*813A=	ENSP00000392617.2:n.*813A=
ENST00000613943.4:c.2298A=	ENSP00000483605.1:n.2298A=
NM_001098426.1:c.*813A=	NP_001091896.1:n.*813A=
XM_005257604.2:c.*813A=	XP_005257661.2:n.*813A=
NM_001330439.1:c.*813A=	NP_001317368.1:n.*813A=
NM_001330440.1:c.*813A=	NP_001317369.1:n.*813A=
NM_001098426.2:c.*813A= MANE Select	NP_001091896.1:n.*813A=
NM_001330440.2:c.*813A=	NP_001317369.1:n.*813A=