Canonical Allele Identifier: CA1826276824
Gene: SLC52A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144359868T= , CM000670.2:g.144359868T= GRCh38
NC_000008.10:g.145583528T= , CM000670.1:g.145583528T= GRCh37
NC_000008.9:g.145554336T= NCBI36
NG_032872.1:g.6312T=
NG_032872.2:g.6312T=

Transcript Alleles

HGVS Amino-acid change
ENST00000329994.7:c.376T= ENSP00000333638.2:p.Cys126=
ENST00000526338.7:c.131-247T= ENSP00000433583.3:n.131-247T=
ENST00000526752.3:c.130+445T= ENSP00000433796.1:n.130+445T=
ENST00000526779.3:c.255+121T= ENSP00000436917.1:n.255+121T=
ENST00000526891.2:c.112T= ENSP00000502670.1:p.Cys38=
ENST00000527078.6:c.376T= ENSP00000434728.1:p.Cys126=
ENST00000532815.2:c.376T= ENSP00000501933.1:p.Cys126=
ENST00000533662.2:c.376T= ENSP00000502274.1:p.Cys126=
ENST00000534725.6:c.376T= ENSP00000431965.2:p.Cys126=
ENST00000643944.2:c.376T= MANE Select ENSP00000496184.2:p.Cys126=
ENST00000674779.1:c.234+142T= ENSP00000501929.1:n.234+142T=
ENST00000674821.1:c.*180T= ENSP00000502219.1:n.*180T=
ENST00000674870.1:c.376T= ENSP00000502406.1:p.Cys126=
ENST00000674929.1:c.131-247T= ENSP00000501554.1:n.131-247T=
ENST00000675121.1:c.376T= ENSP00000501993.1:p.Cys126=
ENST00000675280.1:c.376T= ENSP00000502796.1:p.Cys126=
ENST00000675292.1:c.376T= ENSP00000502652.1:p.Cys126=
ENST00000675597.1:c.131-247T= ENSP00000501973.1:n.131-247T=
ENST00000675787.1:c.376T= ENSP00000502189.1:p.Cys126=
ENST00000675888.1:c.376T= ENSP00000502294.1:p.Cys126=
ENST00000676094.1:c.131-304T= ENSP00000502066.1:n.131-304T=
ENST00000676358.1:c.255+121T= ENSP00000501821.1:n.255+121T=
ENST00000329994.6:c.376T= ENSP00000333638.2:p.Cys126=
ENST00000402965.5:c.376T= ENSP00000385961.1:p.Cys126=
ENST00000526338.5:c.131-247T= ENSP00000433583.1:n.131-247T=
ENST00000526752.1:c.130+445T= ENSP00000433796.1:n.130+445T=
ENST00000526779.1:c.255+121T= ENSP00000436917.1:n.255+121T=
ENST00000526891.1:n.459T=
ENST00000527078.5:c.376T= ENSP00000434728.1:p.Cys126=
ENST00000530047.5:c.376T= ENSP00000435820.1:p.Cys126=
ENST00000532887.5:c.376T= ENSP00000436768.1:p.Cys126=
ENST00000533662.1:n.1075T=
ENST00000534725.5:c.376T= ENSP00000431965.1:p.Cys126=
NM_001253815.1:c.376T= NP_001240744.1:p.Cys126=
NM_001253816.1:c.376T= NP_001240745.1:p.Cys126=
NM_024531.4:c.376T= NP_078807.1:p.Cys126=
NR_045600.1:n.868T=
XM_006716658.1:c.376T= XP_006716721.1:p.Cys126=
XM_006716659.1:c.376T= XP_006716722.1:p.Cys126=
XM_006716660.1:c.376T= XP_006716723.1:p.Cys126=
XM_011517300.1:c.112T= XP_011515602.1:p.Cys38=
NM_001363118.1:c.376T= NP_001350047.1:p.Cys126=
NM_001363120.1:c.376T= NP_001350049.1:p.Cys126=
NM_001363121.1:c.376T= NP_001350050.1:p.Cys126=
NM_001363122.1:c.131-247T= NP_001350051.1:n.131-247T=
XM_011517300.2:c.112T= XP_011515602.1:p.Cys38=
XM_017013821.1:c.131-247T= XP_016869310.1:n.131-247T=
XM_017013822.1:c.131-247T= XP_016869311.1:n.131-247T=
NM_001253815.2:c.376T= NP_001240744.1:p.Cys126=
NM_001253816.2:c.376T= NP_001240745.1:p.Cys126=
NM_001363118.2:c.376T= MANE Select NP_001350047.1:p.Cys126=
NM_001363120.2:c.376T= NP_001350049.1:p.Cys126=
NM_001363121.2:c.376T= NP_001350050.1:p.Cys126=
NM_001363122.2:c.131-247T= NP_001350051.1:n.131-247T=
NM_024531.5:c.376T= NP_078807.1:p.Cys126=
NR_045600.2:n.836T=