Canonical Allele Identifier: CA2145076981

Gene: SLC8A3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.70166361C= , CM000676.2:g.70166361C=	GRCh38
NC_000014.8:g.70633078C= , CM000676.1:g.70633078C=	GRCh37
NC_000014.7:g.69702831C=	NCBI36
NG_047080.1:g.62252G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000528359.6:c.1784+278G=	ENSP00000433531.1:n.1784+278G=
ENST00000705391.1:c.1784+278G=	ENSP00000516120.1:n.1784+278G=
ENST00000356921.7:c.1784+278G= MANE Select	ENSP00000349392.3:n.1784+278G=
ENST00000356921.6:c.1784+278G=	ENSP00000349392.2:n.1784+278G=
ENST00000357887.7:c.1784+278G=	ENSP00000350560.3:n.1784+278G=
ENST00000381269.6:c.1784+278G=	ENSP00000370669.2:n.1784+278G=
ENST00000494208.5:c.1784+278G=	ENSP00000436332.1:n.1784+278G=
ENST00000528359.5:c.1784+278G=	ENSP00000433531.1:n.1784+278G=
ENST00000534137.5:c.1784+278G=	ENSP00000436688.1:n.1784+278G=
NM_033262.4:c.1784+278G=	NP_150287.1:n.1784+278G=
NM_058240.3:c.1784+278G=	NP_489479.1:n.1784+278G=
NM_182932.2:c.1784+278G=	NP_891977.1:n.1784+278G=
NM_183002.2:c.1784+278G=	NP_892114.1:n.1784+278G=
NR_104122.1:n.2538+278G=
XM_005268017.1:c.1784+278G=	XP_005268074.1:n.1784+278G=
XM_005268018.2:c.1253+278G=	XP_005268075.2:n.1253+278G=
XM_011537101.1:c.1784+278G=	XP_011535403.1:n.1784+278G=
XM_011537102.1:c.1784+278G=	XP_011535404.1:n.1784+278G=
XM_017021606.1:c.1784+278G=	XP_016877095.1:n.1784+278G=
XM_017021607.1:c.1784+278G=	XP_016877096.1:n.1784+278G=
XM_017021608.1:c.1784+278G=	XP_016877097.1:n.1784+278G=
XM_017021609.1:c.1784+278G=	XP_016877098.1:n.1784+278G=
XM_017021610.1:c.*80G=	XP_016877099.1:n.*80G=
NM_058240.4:c.1784+278G=	NP_489479.1:n.1784+278G=
NM_182932.3:c.1784+278G= MANE Select	NP_891977.1:n.1784+278G=
NM_183002.3:c.1784+278G=	NP_892114.1:n.1784+278G=
NR_104122.2:n.2419+278G=
NM_033262.5:c.1784+278G=	NP_150287.1:n.1784+278G=