Canonical Allele Identifier: CA2270103293

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832280C= , CM000679.2:g.63832280C=	GRCh38
NC_000017.10:g.61909640C= , CM000679.1:g.61909640C=	GRCh37
NC_000017.9:g.59263372C=	NCBI36
NG_053004.1:g.15712G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2533G=
ENST00000697953.1:n.3106G=
ENST00000698013.1:n.3218G=
ENST00000698014.1:n.3441G=
ENST00000698015.1:n.2534G=
ENST00000698016.1:c.*658G=	ENSP00000513502.1:n.*658G=
ENST00000698017.1:n.2608G=
ENST00000698018.1:n.2739G=
ENST00000698019.1:n.2937G=
ENST00000698020.1:n.2043G=
ENST00000698021.1:c.1952G=
ENST00000698022.1:c.*658G=	ENSP00000513504.1:n.*658G=
ENST00000698023.1:n.2637G=
ENST00000698024.1:n.2499G=
ENST00000698025.1:n.2659G=
ENST00000698026.1:n.1550G=
ENST00000698027.1:c.*875G=	ENSP00000513505.1:n.*875G=
ENST00000698028.1:n.2742G=
ENST00000448276.7:c.*658G= MANE Select	ENSP00000392617.2:n.*658G=
ENST00000448276.6:c.*658G=	ENSP00000392617.2:n.*658G=
ENST00000613943.4:c.2143G=	ENSP00000483605.1:n.2143G=
NM_001098426.1:c.*658G=	NP_001091896.1:n.*658G=
XM_005257604.2:c.*658G=	XP_005257661.2:n.*658G=
NM_001330439.1:c.*658G=	NP_001317368.1:n.*658G=
NM_001330440.1:c.*658G=	NP_001317369.1:n.*658G=
NM_001098426.2:c.*658G= MANE Select	NP_001091896.1:n.*658G=
NM_001330440.2:c.*658G=	NP_001317369.1:n.*658G=