Canonical Allele Identifier: CA2270103059

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832209T= , CM000679.2:g.63832209T=	GRCh38
NC_000017.10:g.61909569T= , CM000679.1:g.61909569T=	GRCh37
NC_000017.9:g.59263301T=	NCBI36
NG_053004.1:g.15783A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2604A=
ENST00000697953.1:n.3177A=
ENST00000698013.1:n.3289A=
ENST00000698014.1:n.3512A=
ENST00000698015.1:n.2605A=
ENST00000698016.1:c.*729A=	ENSP00000513502.1:n.*729A=
ENST00000698017.1:n.2679A=
ENST00000698018.1:n.2810A=
ENST00000698019.1:n.3008A=
ENST00000698020.1:n.2114A=
ENST00000698021.1:c.2023A=
ENST00000698022.1:c.*729A=	ENSP00000513504.1:n.*729A=
ENST00000698023.1:n.2708A=
ENST00000698024.1:n.2570A=
ENST00000698025.1:n.2730A=
ENST00000698026.1:n.1621A=
ENST00000698027.1:c.*946A=	ENSP00000513505.1:n.*946A=
ENST00000698028.1:n.2813A=
ENST00000448276.7:c.*729A= MANE Select	ENSP00000392617.2:n.*729A=
ENST00000448276.6:c.*729A=	ENSP00000392617.2:n.*729A=
ENST00000613943.4:c.2214A=	ENSP00000483605.1:n.2214A=
NM_001098426.1:c.*729A=	NP_001091896.1:n.*729A=
XM_005257604.2:c.*729A=	XP_005257661.2:n.*729A=
NM_001330439.1:c.*729A=	NP_001317368.1:n.*729A=
NM_001330440.1:c.*729A=	NP_001317369.1:n.*729A=
NM_001098426.2:c.*729A= MANE Select	NP_001091896.1:n.*729A=
NM_001330440.2:c.*729A=	NP_001317369.1:n.*729A=