Canonical Allele Identifier: CA2270105629

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837649G= , CM000679.2:g.63837649G=	GRCh38
NC_000017.10:g.61915009G= , CM000679.1:g.61915009G=	GRCh37
NC_000017.9:g.59268741G=	NCBI36
NG_053004.1:g.10343C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.105-24C=
ENST00000698016.1:c.52C=	ENSP00000513502.1:p.Pro18=
ENST00000698022.1:c.34-24C=	ENSP00000513504.1:n.34-24C=
ENST00000698027.1:c.52C=	ENSP00000513505.1:p.Pro18=
ENST00000448276.7:c.217-24C= MANE Select	ENSP00000392617.2:n.217-24C=
ENST00000225742.13:c.-9-24C=	ENSP00000225742.9:n.-9-24C=
ENST00000323347.14:c.73-24C=	ENSP00000318451.10:n.73-24C=
ENST00000448276.6:c.217-24C=	ENSP00000392617.2:n.217-24C=
ENST00000577686.1:n.53-412C=
ENST00000584400.5:c.217-412C=	ENSP00000464503.1:n.217-412C=
ENST00000613943.4:c.106-24C=	ENSP00000483605.1:n.106-24C=
NM_001098426.1:c.217-24C=	NP_001091896.1:n.217-24C=
XM_005257604.2:c.-9-24C=	XP_005257661.2:n.-9-24C=
NM_001330439.1:c.-9-24C=	NP_001317368.1:n.-9-24C=
NM_001330440.1:c.73-24C=	NP_001317369.1:n.73-24C=
NM_001098426.2:c.217-24C= MANE Select	NP_001091896.1:n.217-24C=
NM_001330440.2:c.73-24C=	NP_001317369.1:n.73-24C=