Canonical Allele Identifier: CA2613835832
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392311_61392312insTGTAGATCTCTGTGTTC , CM000673.2:g.61392311_61392312insTGTAGATCTCTGTGTTC GRCh38
NC_000011.9:g.61159783_61159784insTGTAGATCTCTGTGTTC , CM000673.1:g.61159783_61159784insTGTAGATCTCTGTGTTC GRCh37
NC_000011.8:g.60916359_60916360insTGTAGATCTCTGTGTTC NCBI36
NG_032976.1:g.4952_4953insTGTAGATCTCTGTGTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000515837.6:c.-321_-320insTGTAGATCTCTGTGTTC ENSP00000440638.1:n.-321_-320insTGTAGATCTCTGTGTTC
XM_005274039.3:c.-652_-651insTGTAGATCTCTGTGTTC XP_005274096.1:n.-652_-651insTGTAGATCTCTGTGTTC
XM_005274039.4:c.-652_-651insTGTAGATCTCTGTGTTC XP_005274096.1:n.-652_-651insTGTAGATCTCTGTGTTC