Canonical Allele Identifier: CA501202280

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914815A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837455A>T , CM000679.2:g.63837455A>T	GRCh38
NC_000017.10:g.61914815A>T , CM000679.1:g.61914815A>T	GRCh37
NC_000017.9:g.59268547A>T	NCBI36
NG_053004.1:g.10537T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.275T>A
ENST00000698015.1:n.21T>A
ENST00000698016.1:c.246T>A	ENSP00000513502.1:p.Pro82=
ENST00000698021.1:c.50T>A
ENST00000698022.1:c.204T>A	ENSP00000513504.1:p.Pro68=
ENST00000698027.1:c.246T>A	ENSP00000513505.1:p.Pro82=
ENST00000448276.7:c.387T>A MANE Select	ENSP00000392617.2:p.Pro129=
ENST00000225742.13:c.162T>A	ENSP00000225742.9:p.Pro54=
ENST00000323347.14:c.243T>A	ENSP00000318451.10:p.Pro81=
ENST00000448276.6:c.387T>A	ENSP00000392617.2:p.Pro129=
ENST00000577686.1:n.53-218T>A
ENST00000580054.1:c.171T>A	ENSP00000463793.1:p.Pro57=
ENST00000584400.5:c.217-218T>A	ENSP00000464503.1:n.217-218T>A
ENST00000613943.4:c.276T>A	ENSP00000483605.1:p.Pro92=
NM_001098426.1:c.387T>A	NP_001091896.1:p.Pro129=
XM_005257604.2:c.162T>A	XP_005257661.2:p.Pro54=
NM_001330439.1:c.162T>A	NP_001317368.1:p.Pro54=
NM_001330440.1:c.243T>A	NP_001317369.1:p.Pro81=
NM_001098426.2:c.387T>A MANE Select	NP_001091896.1:p.Pro129=
NM_001330440.2:c.243T>A	NP_001317369.1:p.Pro81=