Canonical Allele Identifier: CA2270105603

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837593G= , CM000679.2:g.63837593G=	GRCh38
NC_000017.10:g.61914953G= , CM000679.1:g.61914953G=	GRCh37
NC_000017.9:g.59268685G=	NCBI36
NG_053004.1:g.10399C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.137C=
ENST00000698016.1:c.108C=	ENSP00000513502.1:p.Pro36=
ENST00000698022.1:c.66C=	ENSP00000513504.1:p.Pro22=
ENST00000698027.1:c.108C=	ENSP00000513505.1:p.Pro36=
ENST00000448276.7:c.249C= MANE Select	ENSP00000392617.2:p.Pro83=
ENST00000225742.13:c.24C=	ENSP00000225742.9:p.Pro8=
ENST00000323347.14:c.105C=	ENSP00000318451.10:p.Pro35=
ENST00000448276.6:c.249C=	ENSP00000392617.2:p.Pro83=
ENST00000577686.1:n.53-356C=
ENST00000580054.1:c.33C=	ENSP00000463793.1:p.Pro11=
ENST00000584400.5:c.217-356C=	ENSP00000464503.1:n.217-356C=
ENST00000613943.4:c.138C=	ENSP00000483605.1:p.Pro46=
NM_001098426.1:c.249C=	NP_001091896.1:p.Pro83=
XM_005257604.2:c.24C=	XP_005257661.2:p.Pro8=
NM_001330439.1:c.24C=	NP_001317368.1:p.Pro8=
NM_001330440.1:c.105C=	NP_001317369.1:p.Pro35=
NM_001098426.2:c.249C= MANE Select	NP_001091896.1:p.Pro83=
NM_001330440.2:c.105C=	NP_001317369.1:p.Pro35=