Canonical Allele Identifier: CA2613835857
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392335_61392336insG , CM000673.2:g.61392335_61392336insG GRCh38
NC_000011.9:g.61159807_61159808insG , CM000673.1:g.61159807_61159808insG GRCh37
NC_000011.8:g.60916383_60916384insG NCBI36
NG_032976.1:g.4976_4977insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-297_-296insG ENSP00000440638.1:n.-297_-296insG
XM_005274039.3:c.-628_-627insG XP_005274096.1:n.-628_-627insG
XM_005274039.4:c.-628_-627insG XP_005274096.1:n.-628_-627insG