Canonical Allele Identifier: CA2792319997
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392320_61392321insT , CM000673.2:g.61392320_61392321insT GRCh38
NC_000011.9:g.61159792_61159793insT , CM000673.1:g.61159792_61159793insT GRCh37
NC_000011.8:g.60916368_60916369insT NCBI36
NG_032976.1:g.4961_4962insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-312_-311insT ENSP00000440638.1:n.-312_-311insT
XM_005274039.3:c.-643_-642insT XP_005274096.1:n.-643_-642insT
XM_005274039.4:c.-643_-642insT XP_005274096.1:n.-643_-642insT