Canonical Allele Identifier: CA262994918

Gene: SLC8A3

Linked Data

• dbSNP Id: rs777544172
• gnomAD v4: 14-70166631-T-C
• MyVariant Identifiers: chr14:g.70633348T>C (hg19) ; chr14:g.70166631T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70166631T>C , CM000676.2:g.70166631T>C	GRCh38
NC_000014.8:g.70633348T>C , CM000676.1:g.70633348T>C	GRCh37
NC_000014.7:g.69703101T>C	NCBI36
NG_047080.1:g.61982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528359.6:c.1784+8A>G	ENSP00000433531.1:n.1784+8A>G
ENST00000705391.1:c.1784+8A>G	ENSP00000516120.1:n.1784+8A>G
ENST00000356921.7:c.1784+8A>G MANE Select	ENSP00000349392.3:n.1784+8A>G
ENST00000356921.6:c.1784+8A>G	ENSP00000349392.2:n.1784+8A>G
ENST00000357887.7:c.1784+8A>G	ENSP00000350560.3:n.1784+8A>G
ENST00000381269.6:c.1784+8A>G	ENSP00000370669.2:n.1784+8A>G
ENST00000494208.5:c.1784+8A>G	ENSP00000436332.1:n.1784+8A>G
ENST00000528359.5:c.1784+8A>G	ENSP00000433531.1:n.1784+8A>G
ENST00000534137.5:c.1784+8A>G	ENSP00000436688.1:n.1784+8A>G
NM_033262.4:c.1784+8A>G	NP_150287.1:n.1784+8A>G
NM_058240.3:c.1784+8A>G	NP_489479.1:n.1784+8A>G
NM_182932.2:c.1784+8A>G	NP_891977.1:n.1784+8A>G
NM_183002.2:c.1784+8A>G	NP_892114.1:n.1784+8A>G
NR_104122.1:n.2538+8A>G
XM_005268017.1:c.1784+8A>G	XP_005268074.1:n.1784+8A>G
XM_005268018.2:c.1253+8A>G	XP_005268075.2:n.1253+8A>G
XM_011537101.1:c.1784+8A>G	XP_011535403.1:n.1784+8A>G
XM_011537102.1:c.1784+8A>G	XP_011535404.1:n.1784+8A>G
XM_017021606.1:c.1784+8A>G	XP_016877095.1:n.1784+8A>G
XM_017021607.1:c.1784+8A>G	XP_016877096.1:n.1784+8A>G
XM_017021608.1:c.1784+8A>G	XP_016877097.1:n.1784+8A>G
XM_017021609.1:c.1784+8A>G	XP_016877098.1:n.1784+8A>G
XM_017021610.1:c.1784+8A>G	XP_016877099.1:n.1784+8A>G
NM_058240.4:c.1784+8A>G	NP_489479.1:n.1784+8A>G
NM_182932.3:c.1784+8A>G MANE Select	NP_891977.1:n.1784+8A>G
NM_183002.3:c.1784+8A>G	NP_892114.1:n.1784+8A>G
NR_104122.2:n.2419+8A>G
NM_033262.5:c.1784+8A>G	NP_150287.1:n.1784+8A>G