Canonical Allele Identifier: CA2270105571

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837507A= , CM000679.2:g.63837507A=	GRCh38
NC_000017.10:g.61914867A= , CM000679.1:g.61914867A=	GRCh37
NC_000017.9:g.59268599A=	NCBI36
NG_053004.1:g.10485T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.223T=
ENST00000698016.1:c.194T=	ENSP00000513502.1:p.Met65=
ENST00000698022.1:c.152T=	ENSP00000513504.1:p.Met51=
ENST00000698027.1:c.194T=	ENSP00000513505.1:p.Met65=
ENST00000448276.7:c.335T= MANE Select	ENSP00000392617.2:p.Met112=
ENST00000225742.13:c.110T=	ENSP00000225742.9:p.Met37=
ENST00000323347.14:c.191T=	ENSP00000318451.10:p.Met64=
ENST00000448276.6:c.335T=	ENSP00000392617.2:p.Met112=
ENST00000577686.1:n.53-270T=
ENST00000580054.1:c.119T=	ENSP00000463793.1:p.Met40=
ENST00000584400.5:c.217-270T=	ENSP00000464503.1:n.217-270T=
ENST00000613943.4:c.224T=	ENSP00000483605.1:p.Met75=
NM_001098426.1:c.335T=	NP_001091896.1:p.Met112=
XM_005257604.2:c.110T=	XP_005257661.2:p.Met37=
NM_001330439.1:c.110T=	NP_001317368.1:p.Met37=
NM_001330440.1:c.191T=	NP_001317369.1:p.Met64=
NM_001098426.2:c.335T= MANE Select	NP_001091896.1:p.Met112=
NM_001330440.2:c.191T=	NP_001317369.1:p.Met64=