Canonical Allele Identifier: CA2437472706
Gene: SLC16A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.74422117_74422118delinsTC , CM000685.2:g.74422117_74422118delinsTC GRCh38
NC_000023.10:g.73641952_73641953delinsTC , CM000685.1:g.73641952_73641953delinsTC GRCh37
NC_000023.9:g.73558677_73558678delinsTC NCBI36
NG_011641.1:g.5868_5869delinsTC
NG_011641.2:g.5868_5869delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000587091.6:c.430+50_430+51delinsTC MANE Select ENSP00000465734.1:n.430+50_430+51delinsTC
ENST00000636771.1:c.176+50_176+51delinsTC
ENST00000587091.5:c.430+50_430+51delinsTC ENSP00000465734.1:n.430+50_430+51delinsTC
NM_006517.4:c.430+50_430+51delinsTC NP_006508.2:n.430+50_430+51delinsTC
XM_005262294.1:c.430+50_430+51delinsTC XP_005262351.1:n.430+50_430+51delinsTC
XM_011531015.1:c.430+50_430+51delinsTC XP_011529317.1:n.430+50_430+51delinsTC
NM_006517.5:c.430+50_430+51delinsTC MANE Select NP_006508.2:n.430+50_430+51delinsTC