Canonical Allele Identifier: CA2815123962
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4977089del , CM000682.2:g.4977089del GRCh38
NC_000020.10:g.4957735del , CM000682.1:g.4957735del GRCh37
NC_000020.9:g.4905735del NCBI36
NG_029959.1:g.29413del
NG_029959.2:g.38207del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338244.6:c.-281-6168del MANE Select ENSP00000344322.1:n.-281-6168del
ENST00000338244.5:c.-281-6168del ENSP00000344322.1:n.-281-6168del
ENST00000379333.5:c.-281-6168del ENSP00000368637.1:n.-281-6168del
ENST00000468355.5:n.90-6172del
NM_005116.5:c.-281-6168del NP_005107.4:n.-281-6168del
NM_203327.1:c.-281-6168del NP_976072.1:n.-281-6168del
XM_011529414.1:c.-277-6172del XP_011527716.1:n.-277-6172del
XM_011529417.1:c.-155+24319del XP_011527719.1:n.-155+24319del
NM_005116.6:c.-281-6168del MANE Select NP_005107.4:n.-281-6168del
NM_203327.2:c.-281-6168del NP_976072.1:n.-281-6168del