Canonical Allele Identifier: CA359019316

Gene: EXOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.462275G>A , CM000667.2:g.462275G>A	GRCh38
NC_000005.9:g.462390G>A , CM000667.1:g.462390G>A	GRCh37
NC_000005.8:g.515390G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000512944.6:c.1621G>A MANE Select	ENSP00000425587.1:p.Gly541Ser
ENST00000315013.9:c.1621G>A	ENSP00000323377.5:p.Gly541Ser
ENST00000503889.2:c.1230G>A
ENST00000511015.1:n.560G>A
ENST00000512944.5:c.1621G>A	ENSP00000425587.1:p.Gly541Ser
ENST00000515601.6:c.1276G>A	ENSP00000424404.1:p.Gly426Ser
NM_007277.4:c.1621G>A	NP_009208.2:p.Gly541Ser
XM_011513948.1:c.1621G>A	XP_011512250.1:p.Gly541Ser
XM_011513949.1:c.1621G>A	XP_011512251.1:p.Gly541Ser
XM_011513950.1:c.1621G>A	XP_011512252.1:p.Gly541Ser
XM_011513951.1:c.1276G>A	XP_011512253.1:p.Gly426Ser
NM_007277.5:c.1621G>A MANE Select	NP_009208.2:p.Gly541Ser