Canonical Allele Identifier: CA1977299989
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61397708A= , CM000673.2:g.61397708A= GRCh38
NC_000011.9:g.61165180A= , CM000673.1:g.61165180A= GRCh37
NC_000011.8:g.60921756A= NCBI36
NG_032976.1:g.10349A=

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.230-66A= ENSP00000334844.5:n.230-66A=
ENST00000544795.6:n.507-20A=
ENST00000684926.1:n.246-20A=
ENST00000688959.1:c.-21-74A= ENSP00000509213.1:n.-21-74A=
ENST00000690736.1:c.230-20A= ENSP00000508542.1:n.230-20A=
ENST00000515837.7:c.230-66A= MANE Select ENSP00000440638.1:n.230-66A=
ENST00000334888.9:c.230-66A= ENSP00000334844.5:n.230-66A=
ENST00000398979.7:c.47-66A= ENSP00000381950.3:n.47-66A=
ENST00000515837.6:c.230-66A= ENSP00000440638.1:n.230-66A=
ENST00000544795.5:n.246-20A=
NM_001173990.2:c.230-66A= NP_001167461.1:n.230-66A=
NM_001173991.2:c.230-66A= NP_001167462.1:n.230-66A=
NM_016499.5:c.47-66A= NP_057583.2:n.47-66A=
XM_005274039.3:c.47-66A= XP_005274096.1:n.47-66A=
NM_001330285.1:c.47-66A= NP_001317214.1:n.47-66A=
XM_005274039.4:c.47-66A= XP_005274096.1:n.47-66A=
NM_001173990.3:c.230-66A= MANE Select NP_001167461.1:n.230-66A=
NM_001173991.3:c.230-66A= NP_001167462.1:n.230-66A=
NM_001330285.2:c.47-66A= NP_001317214.1:n.47-66A=
NM_016499.6:c.47-66A= NP_057583.2:n.47-66A=