Canonical Allele Identifier: CA3174842
Gene: EXOC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.447725G>A , CM000667.2:g.447725G>A GRCh38
NC_000005.9:g.447840G>A , CM000667.1:g.447840G>A GRCh37
NC_000005.8:g.500840G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_007277.5:c.337G>A MANE Select NP_009208.2:p.Val113Met
ENST00000512944.6:c.337G>A MANE Select ENSP00000425587.1:p.Val113Met
NM_007277.4:c.337G>A NP_009208.2:p.Val113Met
ENST00000315013.9:c.337G>A ENSP00000323377.5:p.Val113Met
ENST00000512944.5:c.337G>A ENSP00000425587.1:p.Val113Met
ENST00000515601.6:c.337G>A ENSP00000424404.1:p.Val113Met
XM_011513948.1:c.337G>A XP_011512250.1:p.Val113Met
XM_011513949.1:c.337G>A XP_011512251.1:p.Val113Met
XM_011513950.1:c.337G>A XP_011512252.1:p.Val113Met
XM_011513951.1:c.337G>A XP_011512253.1:p.Val113Met