Canonical Allele Identifier: CA2347254839
Gene: SLC23A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.4910964_4910965delinsTA , CM000682.2:g.4910964_4910965delinsTA GRCh38
NC_000020.10:g.4891610_4891611delinsTA , CM000682.1:g.4891610_4891611delinsTA GRCh37
NC_000020.9:g.4839610_4839611delinsTA NCBI36
NG_029959.1:g.95535_95536delinsTA
NG_029959.2:g.104329_104330delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000338244.6:c.207+1915_207+1916delinsTA MANE Select ENSP00000344322.1:n.207+1915_207+1916delinsTA
ENST00000338244.5:c.207+1915_207+1916delinsTA ENSP00000344322.1:n.207+1915_207+1916delinsTA
ENST00000379333.5:c.207+1915_207+1916delinsTA ENSP00000368637.1:n.207+1915_207+1916delinsTA
ENST00000468355.5:n.573+1915_573+1916delinsTA
NM_005116.5:c.207+1915_207+1916delinsTA NP_005107.4:n.207+1915_207+1916delinsTA
NM_203327.1:c.207+1915_207+1916delinsTA NP_976072.1:n.207+1915_207+1916delinsTA
XM_011529414.1:c.207+1915_207+1916delinsTA XP_011527716.1:n.207+1915_207+1916delinsTA
XM_011529415.1:c.207+1915_207+1916delinsTA XP_011527717.1:n.207+1915_207+1916delinsTA
XM_011529416.1:c.207+1915_207+1916delinsTA XP_011527718.1:n.207+1915_207+1916delinsTA
XM_011529417.1:c.207+1915_207+1916delinsTA XP_011527719.1:n.207+1915_207+1916delinsTA
NM_005116.6:c.207+1915_207+1916delinsTA MANE Select NP_005107.4:n.207+1915_207+1916delinsTA
NM_203327.2:c.207+1915_207+1916delinsTA NP_976072.1:n.207+1915_207+1916delinsTA