Canonical Allele Identifier: CA2270105547

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837460T= , CM000679.2:g.63837460T=	GRCh38
NC_000017.10:g.61914820T= , CM000679.1:g.61914820T=	GRCh37
NC_000017.9:g.59268552T=	NCBI36
NG_053004.1:g.10532A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.270A=
ENST00000698015.1:n.16A=
ENST00000698016.1:c.241A=	ENSP00000513502.1:p.Met81=
ENST00000698021.1:c.45A=
ENST00000698022.1:c.199A=	ENSP00000513504.1:p.Met67=
ENST00000698027.1:c.241A=	ENSP00000513505.1:p.Met81=
ENST00000448276.7:c.382A= MANE Select	ENSP00000392617.2:p.Met128=
ENST00000225742.13:c.157A=	ENSP00000225742.9:p.Met53=
ENST00000323347.14:c.238A=	ENSP00000318451.10:p.Met80=
ENST00000448276.6:c.382A=	ENSP00000392617.2:p.Met128=
ENST00000577686.1:n.53-223A=
ENST00000580054.1:c.166A=	ENSP00000463793.1:p.Met56=
ENST00000584400.5:c.217-223A=	ENSP00000464503.1:n.217-223A=
ENST00000613943.4:c.271A=	ENSP00000483605.1:p.Met91=
NM_001098426.1:c.382A=	NP_001091896.1:p.Met128=
XM_005257604.2:c.157A=	XP_005257661.2:p.Met53=
NM_001330439.1:c.157A=	NP_001317368.1:p.Met53=
NM_001330440.1:c.238A=	NP_001317369.1:p.Met80=
NM_001098426.2:c.382A= MANE Select	NP_001091896.1:p.Met128=
NM_001330440.2:c.238A=	NP_001317369.1:p.Met80=