Canonical Allele Identifier: CA400601572

Gene: SMARCD2

Linked Data

• MyVariant Identifiers: chr17:g.61914865C>A (hg19) ; chr17:g.63837505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837505C>A , CM000679.2:g.63837505C>A	GRCh38
NC_000017.10:g.61914865C>A , CM000679.1:g.61914865C>A	GRCh37
NC_000017.9:g.59268597C>A	NCBI36
NG_053004.1:g.10487G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.225G>T
ENST00000698016.1:c.196G>T	ENSP00000513502.1:p.Asp66Tyr
ENST00000698022.1:c.154G>T	ENSP00000513504.1:p.Asp52Tyr
ENST00000698027.1:c.196G>T	ENSP00000513505.1:p.Asp66Tyr
ENST00000448276.7:c.337G>T MANE Select	ENSP00000392617.2:p.Asp113Tyr
ENST00000225742.13:c.112G>T	ENSP00000225742.9:p.Asp38Tyr
ENST00000323347.14:c.193G>T	ENSP00000318451.10:p.Asp65Tyr
ENST00000448276.6:c.337G>T	ENSP00000392617.2:p.Asp113Tyr
ENST00000577686.1:n.53-268G>T
ENST00000580054.1:c.121G>T	ENSP00000463793.1:p.Asp41Tyr
ENST00000584400.5:c.217-268G>T	ENSP00000464503.1:n.217-268G>T
ENST00000613943.4:c.226G>T	ENSP00000483605.1:p.Asp76Tyr
NM_001098426.1:c.337G>T	NP_001091896.1:p.Asp113Tyr
XM_005257604.2:c.112G>T	XP_005257661.2:p.Asp38Tyr
NM_001330439.1:c.112G>T	NP_001317368.1:p.Asp38Tyr
NM_001330440.1:c.193G>T	NP_001317369.1:p.Asp65Tyr
NM_001098426.2:c.337G>T MANE Select	NP_001091896.1:p.Asp113Tyr
NM_001330440.2:c.193G>T	NP_001317369.1:p.Asp65Tyr