Canonical Allele Identifier: CA400601754

Gene: SMARCD2

Linked Data

• gnomAD v4: 17-63837596-C-G
• MyVariant Identifiers: chr17:g.61914956C>G (hg19) ; chr17:g.63837596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837596C>G , CM000679.2:g.63837596C>G	GRCh38
NC_000017.10:g.61914956C>G , CM000679.1:g.61914956C>G	GRCh37
NC_000017.9:g.59268688C>G	NCBI36
NG_053004.1:g.10396G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.134G>C
ENST00000698016.1:c.105G>C	ENSP00000513502.1:p.Met35Ile
ENST00000698022.1:c.63G>C	ENSP00000513504.1:p.Met21Ile
ENST00000698027.1:c.105G>C	ENSP00000513505.1:p.Met35Ile
ENST00000448276.7:c.246G>C MANE Select	ENSP00000392617.2:p.Met82Ile
ENST00000225742.13:c.21G>C	ENSP00000225742.9:p.Met7Ile
ENST00000323347.14:c.102G>C	ENSP00000318451.10:p.Met34Ile
ENST00000448276.6:c.246G>C	ENSP00000392617.2:p.Met82Ile
ENST00000577686.1:n.53-359G>C
ENST00000580054.1:c.30G>C	ENSP00000463793.1:p.Met10Ile
ENST00000584400.5:c.217-359G>C	ENSP00000464503.1:n.217-359G>C
ENST00000613943.4:c.135G>C	ENSP00000483605.1:p.Met45Ile
NM_001098426.1:c.246G>C	NP_001091896.1:p.Met82Ile
XM_005257604.2:c.21G>C	XP_005257661.2:p.Met7Ile
NM_001330439.1:c.21G>C	NP_001317368.1:p.Met7Ile
NM_001330440.1:c.102G>C	NP_001317369.1:p.Met34Ile
NM_001098426.2:c.246G>C MANE Select	NP_001091896.1:p.Met82Ile
NM_001330440.2:c.102G>C	NP_001317369.1:p.Met34Ile