Canonical Allele Identifier: CA2270105563

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837495C= , CM000679.2:g.63837495C=	GRCh38
NC_000017.10:g.61914855C= , CM000679.1:g.61914855C=	GRCh37
NC_000017.9:g.59268587C=	NCBI36
NG_053004.1:g.10497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.235G=
ENST00000698016.1:c.206G=	ENSP00000513502.1:p.Arg69=
ENST00000698021.1:c.10G=
ENST00000698022.1:c.164G=	ENSP00000513504.1:p.Arg55=
ENST00000698027.1:c.206G=	ENSP00000513505.1:p.Arg69=
ENST00000448276.7:c.347G= MANE Select	ENSP00000392617.2:p.Arg116=
ENST00000225742.13:c.122G=	ENSP00000225742.9:p.Arg41=
ENST00000323347.14:c.203G=	ENSP00000318451.10:p.Arg68=
ENST00000448276.6:c.347G=	ENSP00000392617.2:p.Arg116=
ENST00000577686.1:n.53-258G=
ENST00000580054.1:c.131G=	ENSP00000463793.1:p.Arg44=
ENST00000584400.5:c.217-258G=	ENSP00000464503.1:n.217-258G=
ENST00000613943.4:c.236G=	ENSP00000483605.1:p.Arg79=
NM_001098426.1:c.347G=	NP_001091896.1:p.Arg116=
XM_005257604.2:c.122G=	XP_005257661.2:p.Arg41=
NM_001330439.1:c.122G=	NP_001317368.1:p.Arg41=
NM_001330440.1:c.203G=	NP_001317369.1:p.Arg68=
NM_001098426.2:c.347G= MANE Select	NP_001091896.1:p.Arg116=
NM_001330440.2:c.203G=	NP_001317369.1:p.Arg68=