Canonical Allele Identifier: CA2270102997

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63832094G= , CM000679.2:g.63832094G=	GRCh38
NC_000017.10:g.61909454G= , CM000679.1:g.61909454G=	GRCh37
NC_000017.9:g.59263186G=	NCBI36
NG_053004.1:g.15898C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.3292C=
ENST00000698013.1:n.3404C=
ENST00000698014.1:n.3627C=
ENST00000698015.1:n.2720C=
ENST00000698016.1:c.*844C=	ENSP00000513502.1:n.*844C=
ENST00000698017.1:n.2794C=
ENST00000448276.7:c.*844C= MANE Select	ENSP00000392617.2:n.*844C=
ENST00000448276.6:c.*844C=	ENSP00000392617.2:n.*844C=
ENST00000613943.4:c.2329C=	ENSP00000483605.1:n.2329C=
NM_001098426.1:c.*844C=	NP_001091896.1:n.*844C=
XM_005257604.2:c.*844C=	XP_005257661.2:n.*844C=
NM_001330439.1:c.*844C=	NP_001317368.1:n.*844C=
NM_001330440.1:c.*844C=	NP_001317369.1:n.*844C=
NM_001098426.2:c.*844C= MANE Select	NP_001091896.1:n.*844C=
NM_001330440.2:c.*844C=	NP_001317369.1:n.*844C=