Canonical Allele Identifier: CA501202308

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914836G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837476G>C , CM000679.2:g.63837476G>C	GRCh38
NC_000017.10:g.61914836G>C , CM000679.1:g.61914836G>C	GRCh37
NC_000017.9:g.59268568G>C	NCBI36
NG_053004.1:g.10516C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.254C>G
ENST00000698016.1:c.225C>G	ENSP00000513502.1:p.Pro75=
ENST00000698021.1:c.29C>G
ENST00000698022.1:c.183C>G	ENSP00000513504.1:p.Pro61=
ENST00000698027.1:c.225C>G	ENSP00000513505.1:p.Pro75=
ENST00000448276.7:c.366C>G MANE Select	ENSP00000392617.2:p.Pro122=
ENST00000225742.13:c.141C>G	ENSP00000225742.9:p.Pro47=
ENST00000323347.14:c.222C>G	ENSP00000318451.10:p.Pro74=
ENST00000448276.6:c.366C>G	ENSP00000392617.2:p.Pro122=
ENST00000577686.1:n.53-239C>G
ENST00000580054.1:c.150C>G	ENSP00000463793.1:p.Pro50=
ENST00000584400.5:c.217-239C>G	ENSP00000464503.1:n.217-239C>G
ENST00000613943.4:c.255C>G	ENSP00000483605.1:p.Pro85=
NM_001098426.1:c.366C>G	NP_001091896.1:p.Pro122=
XM_005257604.2:c.141C>G	XP_005257661.2:p.Pro47=
NM_001330439.1:c.141C>G	NP_001317368.1:p.Pro47=
NM_001330440.1:c.222C>G	NP_001317369.1:p.Pro74=
NM_001098426.2:c.366C>G MANE Select	NP_001091896.1:p.Pro122=
NM_001330440.2:c.222C>G	NP_001317369.1:p.Pro74=