Canonical Allele Identifier: CA1977295368
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392309_61392310delinsTG , CM000673.2:g.61392309_61392310delinsTG GRCh38
NC_000011.9:g.61159781_61159782delinsTG , CM000673.1:g.61159781_61159782delinsTG GRCh37
NC_000011.8:g.60916357_60916358delinsTG NCBI36
NG_032976.1:g.4950_4951delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-323_-322delinsTG ENSP00000440638.1:n.-323_-322delinsTG
XM_005274039.3:c.-654_-653delinsTG XP_005274096.1:n.-654_-653delinsTG
XM_005274039.4:c.-654_-653delinsTG XP_005274096.1:n.-654_-653delinsTG