Canonical Allele Identifier: CA2270105579

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837526C= , CM000679.2:g.63837526C=	GRCh38
NC_000017.10:g.61914886C= , CM000679.1:g.61914886C=	GRCh37
NC_000017.9:g.59268618C=	NCBI36
NG_053004.1:g.10466G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.204G=
ENST00000698016.1:c.175G=	ENSP00000513502.1:p.Gly59=
ENST00000698022.1:c.133G=	ENSP00000513504.1:p.Gly45=
ENST00000698027.1:c.175G=	ENSP00000513505.1:p.Gly59=
ENST00000448276.7:c.316G= MANE Select	ENSP00000392617.2:p.Gly106=
ENST00000225742.13:c.91G=	ENSP00000225742.9:p.Gly31=
ENST00000323347.14:c.172G=	ENSP00000318451.10:p.Gly58=
ENST00000448276.6:c.316G=	ENSP00000392617.2:p.Gly106=
ENST00000577686.1:n.53-289G=
ENST00000580054.1:c.100G=	ENSP00000463793.1:p.Gly34=
ENST00000584400.5:c.217-289G=	ENSP00000464503.1:n.217-289G=
ENST00000613943.4:c.205G=	ENSP00000483605.1:p.Gly69=
NM_001098426.1:c.316G=	NP_001091896.1:p.Gly106=
XM_005257604.2:c.91G=	XP_005257661.2:p.Gly31=
NM_001330439.1:c.91G=	NP_001317368.1:p.Gly31=
NM_001330440.1:c.172G=	NP_001317369.1:p.Gly58=
NM_001098426.2:c.316G= MANE Select	NP_001091896.1:p.Gly106=
NM_001330440.2:c.172G=	NP_001317369.1:p.Gly58=