Canonical Allele Identifier: CA2574840979
Gene: TMEM216 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61393144A>T , CM000673.2:g.61393144A>T GRCh38
NC_000011.9:g.61160616A>T , CM000673.1:g.61160616A>T GRCh37
NC_000011.8:g.60917192A>T NCBI36
NG_032976.1:g.5785A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.35-87A>T ENSP00000334844.5:n.35-87A>T
ENST00000544795.6:n.312-87A>T
ENST00000684926.1:n.51-87A>T
ENST00000688959.1:c.-225-87A>T ENSP00000509213.1:n.-225-87A>T
ENST00000690736.1:c.35-87A>T ENSP00000508542.1:n.35-87A>T
ENST00000515837.7:c.35-87A>T MANE Select ENSP00000440638.1:n.35-87A>T
ENST00000334888.9:c.35-87A>T ENSP00000334844.5:n.35-87A>T
ENST00000398979.7:c.-149-87A>T ENSP00000381950.3:n.-149-87A>T
ENST00000515837.6:c.35-87A>T ENSP00000440638.1:n.35-87A>T
ENST00000541473.1:n.49-87A>T
ENST00000544795.5:n.51-87A>T
NM_001173990.2:c.35-87A>T NP_001167461.1:n.35-87A>T
NM_001173991.2:c.35-87A>T NP_001167462.1:n.35-87A>T
NM_016499.5:c.-149-87A>T NP_057583.2:n.-149-87A>T
XM_005274039.3:c.-149-87A>T XP_005274096.1:n.-149-87A>T
NM_001330285.1:c.-149-87A>T NP_001317214.1:n.-149-87A>T
XM_005274039.4:c.-149-87A>T XP_005274096.1:n.-149-87A>T
NM_001173990.3:c.35-87A>T MANE Select NP_001167461.1:n.35-87A>T
NM_001173991.3:c.35-87A>T NP_001167462.1:n.35-87A>T
NM_001330285.2:c.-149-87A>T NP_001317214.1:n.-149-87A>T
NM_016499.6:c.-149-87A>T NP_057583.2:n.-149-87A>T