Canonical Allele Identifier: CA2270105570

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837504T= , CM000679.2:g.63837504T=	GRCh38
NC_000017.10:g.61914864T= , CM000679.1:g.61914864T=	GRCh37
NC_000017.9:g.59268596T=	NCBI36
NG_053004.1:g.10488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.226A=
ENST00000698016.1:c.197A=	ENSP00000513502.1:p.Asp66=
ENST00000698021.1:c.1A=
ENST00000698022.1:c.155A=	ENSP00000513504.1:p.Asp52=
ENST00000698027.1:c.197A=	ENSP00000513505.1:p.Asp66=
ENST00000448276.7:c.338A= MANE Select	ENSP00000392617.2:p.Asp113=
ENST00000225742.13:c.113A=	ENSP00000225742.9:p.Asp38=
ENST00000323347.14:c.194A=	ENSP00000318451.10:p.Asp65=
ENST00000448276.6:c.338A=	ENSP00000392617.2:p.Asp113=
ENST00000577686.1:n.53-267A=
ENST00000580054.1:c.122A=	ENSP00000463793.1:p.Asp41=
ENST00000584400.5:c.217-267A=	ENSP00000464503.1:n.217-267A=
ENST00000613943.4:c.227A=	ENSP00000483605.1:p.Asp76=
NM_001098426.1:c.338A=	NP_001091896.1:p.Asp113=
XM_005257604.2:c.113A=	XP_005257661.2:p.Asp38=
NM_001330439.1:c.113A=	NP_001317368.1:p.Asp38=
NM_001330440.1:c.194A=	NP_001317369.1:p.Asp65=
NM_001098426.2:c.338A= MANE Select	NP_001091896.1:p.Asp113=
NM_001330440.2:c.194A=	NP_001317369.1:p.Asp65=