Canonical Allele Identifier: CA265955102

Gene: SYNE3

Linked Data

• dbSNP Id: rs549597692
• gnomAD v3: 14-95425885-T-C
• gnomAD v4: 14-95425885-T-C
• MyVariant Identifiers: chr14:g.95892222T>C (hg19) ; chr14:g.95425885T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.95425885T>C , CM000676.2:g.95425885T>C	GRCh38
NC_000014.8:g.95892222T>C , CM000676.1:g.95892222T>C	GRCh37
NC_000014.7:g.94961975T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682763.1:c.2727+6194A>G MANE Select	ENSP00000507501.1:n.2727+6194A>G
ENST00000334258.9:c.2727+6194A>G	ENSP00000334308.4:n.2727+6194A>G
ENST00000554873.5:c.1998+6194A>G	ENSP00000452154.1:n.1998+6194A>G
ENST00000557275.5:c.2712+6194A>G	ENSP00000450562.1:n.2712+6194A>G
NM_152592.3:c.2727+6194A>G	NP_689805.3:n.2727+6194A>G
XM_005267376.3:c.2916+6194A>G	XP_005267433.2:n.2916+6194A>G
XM_005267377.2:c.2727+6194A>G	XP_005267434.1:n.2727+6194A>G
XM_006720063.2:c.2727+6194A>G	XP_006720126.1:n.2727+6194A>G
XM_011536513.1:c.2901+6194A>G	XP_011534815.1:n.2901+6194A>G
XM_011536514.1:c.2916+6194A>G	XP_011534816.1:n.2916+6194A>G
XM_011536515.1:c.2751+6194A>G	XP_011534817.1:n.2751+6194A>G
NM_001363692.1:c.2712+6194A>G	NP_001350621.1:n.2712+6194A>G
NM_152592.5:c.2727+6194A>G	NP_689805.3:n.2727+6194A>G
XM_005267377.4:c.2727+6194A>G	XP_005267434.1:n.2727+6194A>G
XM_006720063.4:c.2727+6194A>G	XP_006720126.1:n.2727+6194A>G
XM_011536515.3:c.2751+6194A>G	XP_011534817.1:n.2751+6194A>G
NM_001363692.2:c.2712+6194A>G	NP_001350621.1:n.2712+6194A>G
NM_152592.6:c.2727+6194A>G MANE Select	NP_689805.3:n.2727+6194A>G