Canonical Allele Identifier: CA2270103072

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832434G= , CM000679.2:g.63832434G=	GRCh38
NC_000017.10:g.61909794G= , CM000679.1:g.61909794G=	GRCh37
NC_000017.9:g.59263526G=	NCBI36
NG_053004.1:g.15558C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2379C=
ENST00000697953.1:n.2952C=
ENST00000698013.1:n.3064C=
ENST00000698014.1:n.3287C=
ENST00000698015.1:n.2380C=
ENST00000698016.1:c.*504C=	ENSP00000513502.1:n.*504C=
ENST00000698017.1:n.2454C=
ENST00000698018.1:n.2585C=
ENST00000698019.1:n.2783C=
ENST00000698020.1:n.1889C=
ENST00000698021.1:c.1798C=
ENST00000698022.1:c.*504C=	ENSP00000513504.1:n.*504C=
ENST00000698023.1:n.2483C=
ENST00000698024.1:n.2345C=
ENST00000698025.1:n.2505C=
ENST00000698026.1:n.1396C=
ENST00000698027.1:c.*721C=	ENSP00000513505.1:n.*721C=
ENST00000698028.1:n.2588C=
ENST00000698029.1:n.3317C=
ENST00000448276.7:c.*504C= MANE Select	ENSP00000392617.2:n.*504C=
ENST00000448276.6:c.*504C=	ENSP00000392617.2:n.*504C=
ENST00000613943.4:c.1989C=	ENSP00000483605.1:n.1989C=
NM_001098426.1:c.*504C=	NP_001091896.1:n.*504C=
XM_005257604.2:c.*504C=	XP_005257661.2:n.*504C=
NM_001330439.1:c.*504C=	NP_001317368.1:n.*504C=
NM_001330440.1:c.*504C=	NP_001317369.1:n.*504C=
NM_001098426.2:c.*504C= MANE Select	NP_001091896.1:n.*504C=
NM_001330440.2:c.*504C=	NP_001317369.1:n.*504C=