Canonical Allele Identifier: CA1752584936

Gene: SMARCD3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.151253792G= , CM000669.2:g.151253792G=	GRCh38
NC_000007.13:g.150950878G= , CM000669.1:g.150950878G=	GRCh37
NC_000007.12:g.150581811G=	NCBI36
NG_029468.1:g.28354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356800.6:c.40-8121C=	ENSP00000349254.2:n.40-8121C=
ENST00000392811.6:c.40-8121C=	ENSP00000376558.2:n.40-8121C=
ENST00000469154.5:c.71-10091C=	ENSP00000417908.1:n.71-10091C=
ENST00000477169.5:n.184+503C=
ENST00000491651.1:c.40-8121C=	ENSP00000419886.1:n.40-8121C=
NM_001003802.1:c.40-8121C=	NP_001003802.1:n.40-8121C=
NM_003078.3:c.40-8121C=	NP_003069.2:n.40-8121C=
XM_011516521.1:c.-16-10091C=	XP_011514823.1:n.-16-10091C=
XR_928174.1:n.717-521G=
XM_011516521.2:c.-16-10091C=	XP_011514823.1:n.-16-10091C=
XM_024446887.1:c.40-8121C=	XP_024302655.1:n.40-8121C=
XM_024446888.1:c.-16-10091C=	XP_024302656.1:n.-16-10091C=
XM_024446889.1:c.-221-10091C=	XP_024302657.1:n.-221-10091C=
NM_003078.4:c.40-8121C=	NP_003069.2:n.40-8121C=
NM_001003802.2:c.40-8121C=	NP_001003802.1:n.40-8121C=