Canonical Allele Identifier: CA2270105518

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837406A= , CM000679.2:g.63837406A=	GRCh38
NC_000017.10:g.61914766A= , CM000679.1:g.61914766A=	GRCh37
NC_000017.9:g.59268498A=	NCBI36
NG_053004.1:g.10586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.324T=
ENST00000698015.1:n.35+35T=
ENST00000698016.1:c.260+35T=	ENSP00000513502.1:n.260+35T=
ENST00000698020.1:n.22T=
ENST00000698021.1:c.64+35T=
ENST00000698022.1:c.218+35T=	ENSP00000513504.1:n.218+35T=
ENST00000698027.1:c.260+35T=	ENSP00000513505.1:n.260+35T=
ENST00000448276.7:c.401+35T= MANE Select	ENSP00000392617.2:n.401+35T=
ENST00000225742.13:c.176+35T=	ENSP00000225742.9:n.176+35T=
ENST00000323347.14:c.257+35T=	ENSP00000318451.10:n.257+35T=
ENST00000448276.6:c.401+35T=	ENSP00000392617.2:n.401+35T=
ENST00000577686.1:n.53-169T=
ENST00000580054.1:c.185+35T=	ENSP00000463793.1:n.185+35T=
ENST00000584400.5:c.217-169T=	ENSP00000464503.1:n.217-169T=
ENST00000613943.4:c.290+35T=	ENSP00000483605.1:n.290+35T=
NM_001098426.1:c.401+35T=	NP_001091896.1:n.401+35T=
XM_005257604.2:c.176+35T=	XP_005257661.2:n.176+35T=
NM_001330439.1:c.176+35T=	NP_001317368.1:n.176+35T=
NM_001330440.1:c.257+35T=	NP_001317369.1:n.257+35T=
NM_001098426.2:c.401+35T= MANE Select	NP_001091896.1:n.401+35T=
NM_001330440.2:c.257+35T=	NP_001317369.1:n.257+35T=