Canonical Allele Identifier: CA1979659423
Gene: SLC29A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.66371579C= , CM000673.2:g.66371579C= GRCh38
NC_000011.9:g.66139050C= , CM000673.1:g.66139050C= GRCh37
NC_000011.8:g.65895626C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001532.3:c.13G= MANE Select NP_001523.2:p.Asp5=
ENST00000357440.7:c.13G= MANE Select ENSP00000350024.2:p.Asp5=
NM_001300868.1:c.13G= NP_001287797.1:p.Asp5=
NM_001300868.2:c.13G= NP_001287797.1:p.Asp5=
NM_001300869.1:c.13G= NP_001287798.1:p.Asp5=
NM_001300869.2:c.13G= NP_001287798.1:p.Asp5=
NM_001532.2:c.13G= NP_001523.2:p.Asp5=
NR_125343.1:n.242G=
NR_125343.2:n.182G=
ENST00000311161.11:c.13G= ENSP00000311250.7:p.Asp5=
ENST00000357440.6:c.13G= ENSP00000350024.2:p.Asp5=
ENST00000540386.5:c.13G= ENSP00000444870.1:p.Asp5=
ENST00000541567.5:c.13G= ENSP00000442116.1:p.Asp5=
ENST00000544554.5:c.13G= ENSP00000439456.1:p.Asp5=
ENST00000546034.1:c.13G= ENSP00000440329.1:p.Asp5=
ENST00000619145.4:c.13G= ENSP00000481944.1:p.Asp5=
XM_011544973.1:c.13G= XP_011543275.1:p.Asp5=
XM_011544974.1:c.13G= XP_011543276.1:p.Asp5=
XM_011544975.1:c.13G= XP_011543277.1:p.Asp5=
XM_011544976.1:c.13G= XP_011543278.1:p.Asp5=
XM_011544977.1:c.13G= XP_011543279.1:p.Asp5=
XM_011544978.1:c.13G= XP_011543280.1:p.Asp5=
XM_011544979.1:c.13G= XP_011543281.1:p.Asp5=
XM_011544980.1:c.13G= XP_011543282.1:p.Asp5=
XM_011544981.1:c.-283G= XP_011543283.1:n.-283G=
XM_011544982.1:c.13G= XP_011543284.1:p.Asp5=
XM_017017632.1:c.13G= XP_016873121.1:p.Asp5=
XM_017017633.2:c.13G= XP_016873122.1:p.Asp5=
XM_017017636.2:c.13G= XP_016873125.1:p.Asp5=
XM_024448461.1:c.13G= XP_024304229.1:p.Asp5=
XM_024448462.1:c.-437G= XP_024304230.1:n.-437G=
XM_024448463.1:c.13G= XP_024304231.1:p.Asp5=
XM_024448464.1:c.13G= XP_024304232.1:p.Asp5=
XM_024448465.1:c.13G= XP_024304233.1:p.Asp5=
XR_001747842.1:n.393G=
XR_001747844.2:n.771G=
XR_001747845.2:n.771G=
XR_949900.1:n.785G=