Canonical Allele Identifier: CA1977299984
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61397701A= , CM000673.2:g.61397701A= GRCh38
NC_000011.9:g.61165173A= , CM000673.1:g.61165173A= GRCh37
NC_000011.8:g.60921749A= NCBI36
NG_032976.1:g.10342A=

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.230-73A= ENSP00000334844.5:n.230-73A=
ENST00000544795.6:n.507-27A=
ENST00000684926.1:n.246-27A=
ENST00000688959.1:c.-21-81A= ENSP00000509213.1:n.-21-81A=
ENST00000690736.1:c.230-27A= ENSP00000508542.1:n.230-27A=
ENST00000515837.7:c.230-73A= MANE Select ENSP00000440638.1:n.230-73A=
ENST00000334888.9:c.230-73A= ENSP00000334844.5:n.230-73A=
ENST00000398979.7:c.47-73A= ENSP00000381950.3:n.47-73A=
ENST00000515837.6:c.230-73A= ENSP00000440638.1:n.230-73A=
ENST00000544795.5:n.246-27A=
NM_001173990.2:c.230-73A= NP_001167461.1:n.230-73A=
NM_001173991.2:c.230-73A= NP_001167462.1:n.230-73A=
NM_016499.5:c.47-73A= NP_057583.2:n.47-73A=
XM_005274039.3:c.47-73A= XP_005274096.1:n.47-73A=
NM_001330285.1:c.47-73A= NP_001317214.1:n.47-73A=
XM_005274039.4:c.47-73A= XP_005274096.1:n.47-73A=
NM_001173990.3:c.230-73A= MANE Select NP_001167461.1:n.230-73A=
NM_001173991.3:c.230-73A= NP_001167462.1:n.230-73A=
NM_001330285.2:c.47-73A= NP_001317214.1:n.47-73A=
NM_016499.6:c.47-73A= NP_057583.2:n.47-73A=