Canonical Allele Identifier: CA2270103009

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832115A= , CM000679.2:g.63832115A=	GRCh38
NC_000017.10:g.61909475A= , CM000679.1:g.61909475A=	GRCh37
NC_000017.9:g.59263207A=	NCBI36
NG_053004.1:g.15877T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3271T=
ENST00000698013.1:n.3383T=
ENST00000698014.1:n.3606T=
ENST00000698015.1:n.2699T=
ENST00000698016.1:c.*823T=	ENSP00000513502.1:n.*823T=
ENST00000698017.1:n.2773T=
ENST00000698018.1:n.2904T=
ENST00000698019.1:n.3102T=
ENST00000698020.1:n.2208T=
ENST00000698021.1:c.2117T=
ENST00000698022.1:c.*823T=	ENSP00000513504.1:n.*823T=
ENST00000698023.1:n.2802T=
ENST00000698024.1:n.2664T=
ENST00000448276.7:c.*823T= MANE Select	ENSP00000392617.2:n.*823T=
ENST00000448276.6:c.*823T=	ENSP00000392617.2:n.*823T=
ENST00000613943.4:c.2308T=	ENSP00000483605.1:n.2308T=
NM_001098426.1:c.*823T=	NP_001091896.1:n.*823T=
XM_005257604.2:c.*823T=	XP_005257661.2:n.*823T=
NM_001330439.1:c.*823T=	NP_001317368.1:n.*823T=
NM_001330440.1:c.*823T=	NP_001317369.1:n.*823T=
NM_001098426.2:c.*823T= MANE Select	NP_001091896.1:n.*823T=
NM_001330440.2:c.*823T=	NP_001317369.1:n.*823T=