Canonical Allele Identifier: CA2270103097

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832483C= , CM000679.2:g.63832483C=	GRCh38
NC_000017.10:g.61909843C= , CM000679.1:g.61909843C=	GRCh37
NC_000017.9:g.59263575C=	NCBI36
NG_053004.1:g.15509G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584483.6:n.2330G=
ENST00000697953.1:n.2903G=
ENST00000698013.1:n.3015G=
ENST00000698014.1:n.3238G=
ENST00000698015.1:n.2331G=
ENST00000698016.1:c.*455G=	ENSP00000513502.1:n.*455G=
ENST00000698017.1:n.2405G=
ENST00000698018.1:n.2536G=
ENST00000698019.1:n.2734G=
ENST00000698020.1:n.1840G=
ENST00000698021.1:c.1749G=
ENST00000698022.1:c.*455G=	ENSP00000513504.1:n.*455G=
ENST00000698023.1:n.2434G=
ENST00000698024.1:n.2296G=
ENST00000698025.1:n.2456G=
ENST00000698026.1:n.1347G=
ENST00000698027.1:c.*672G=	ENSP00000513505.1:n.*672G=
ENST00000698028.1:n.2539G=
ENST00000698029.1:n.3268G=
ENST00000448276.7:c.*455G= MANE Select	ENSP00000392617.2:n.*455G=
ENST00000448276.6:c.*455G=	ENSP00000392617.2:n.*455G=
ENST00000613943.4:c.1940G=	ENSP00000483605.1:n.1940G=
NM_001098426.1:c.*455G=	NP_001091896.1:n.*455G=
XM_005257604.2:c.*455G=	XP_005257661.2:n.*455G=
NM_001330439.1:c.*455G=	NP_001317368.1:n.*455G=
NM_001330440.1:c.*455G=	NP_001317369.1:n.*455G=
NM_001098426.2:c.*455G= MANE Select	NP_001091896.1:n.*455G=
NM_001330440.2:c.*455G=	NP_001317369.1:n.*455G=