Canonical Allele Identifier: CA1977295472
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392407C= , CM000673.2:g.61392407C= GRCh38
NC_000011.9:g.61159879C= , CM000673.1:g.61159879C= GRCh37
NC_000011.8:g.60916455C= NCBI36
NG_032976.1:g.5048C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-225C= ENSP00000334844.5:n.-225C=
ENST00000398979.7:c.-422C= ENSP00000381950.3:n.-422C=
ENST00000515837.6:c.-225C= ENSP00000440638.1:n.-225C=
NM_001173990.2:c.-225C= NP_001167461.1:n.-225C=
NM_001173991.2:c.-225C= NP_001167462.1:n.-225C=
NM_016499.5:c.-422C= NP_057583.2:n.-422C=
XM_005274039.3:c.-556C= XP_005274096.1:n.-556C=
NM_001330285.1:c.-422C= NP_001317214.1:n.-422C=
XM_005274039.4:c.-556C= XP_005274096.1:n.-556C=