Canonical Allele Identifier: CA2270105551

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837477G= , CM000679.2:g.63837477G=	GRCh38
NC_000017.10:g.61914837G= , CM000679.1:g.61914837G=	GRCh37
NC_000017.9:g.59268569G=	NCBI36
NG_053004.1:g.10515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.253C=
ENST00000698016.1:c.224C=	ENSP00000513502.1:p.Pro75=
ENST00000698021.1:c.28C=
ENST00000698022.1:c.182C=	ENSP00000513504.1:p.Pro61=
ENST00000698027.1:c.224C=	ENSP00000513505.1:p.Pro75=
ENST00000448276.7:c.365C= MANE Select	ENSP00000392617.2:p.Pro122=
ENST00000225742.13:c.140C=	ENSP00000225742.9:p.Pro47=
ENST00000323347.14:c.221C=	ENSP00000318451.10:p.Pro74=
ENST00000448276.6:c.365C=	ENSP00000392617.2:p.Pro122=
ENST00000577686.1:n.53-240C=
ENST00000580054.1:c.149C=	ENSP00000463793.1:p.Pro50=
ENST00000584400.5:c.217-240C=	ENSP00000464503.1:n.217-240C=
ENST00000613943.4:c.254C=	ENSP00000483605.1:p.Pro85=
NM_001098426.1:c.365C=	NP_001091896.1:p.Pro122=
XM_005257604.2:c.140C=	XP_005257661.2:p.Pro47=
NM_001330439.1:c.140C=	NP_001317368.1:p.Pro47=
NM_001330440.1:c.221C=	NP_001317369.1:p.Pro74=
NM_001098426.2:c.365C= MANE Select	NP_001091896.1:p.Pro122=
NM_001330440.2:c.221C=	NP_001317369.1:p.Pro74=