Canonical Allele Identifier: CA2839730441

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397754C>A , CM000673.2:g.61397754C>A	GRCh38
NC_000011.9:g.61165226C>A , CM000673.1:g.61165226C>A	GRCh37
NC_000011.8:g.60921802C>A	NCBI36
NG_032976.1:g.10395C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.230-20C>A	ENSP00000334844.5:n.230-20C>A
ENST00000544795.6:n.533C>A
ENST00000684926.1:n.272C>A
ENST00000688959.1:c.-21-28C>A	ENSP00000509213.1:n.-21-28C>A
ENST00000690736.1:c.256C>A	ENSP00000508542.1:p.Pro86Thr
ENST00000515837.7:c.230-20C>A MANE Select	ENSP00000440638.1:n.230-20C>A
ENST00000334888.9:c.230-20C>A	ENSP00000334844.5:n.230-20C>A
ENST00000398979.7:c.47-20C>A	ENSP00000381950.3:n.47-20C>A
ENST00000515837.6:c.230-20C>A	ENSP00000440638.1:n.230-20C>A
ENST00000544795.5:n.272C>A
NM_001173990.2:c.230-20C>A	NP_001167461.1:n.230-20C>A
NM_001173991.2:c.230-20C>A	NP_001167462.1:n.230-20C>A
NM_016499.5:c.47-20C>A	NP_057583.2:n.47-20C>A
XM_005274039.3:c.47-20C>A	XP_005274096.1:n.47-20C>A
NM_001330285.1:c.47-20C>A	NP_001317214.1:n.47-20C>A
XM_005274039.4:c.47-20C>A	XP_005274096.1:n.47-20C>A
NM_001173990.3:c.230-20C>A MANE Select	NP_001167461.1:n.230-20C>A
NM_001173991.3:c.230-20C>A	NP_001167462.1:n.230-20C>A
NM_001330285.2:c.47-20C>A	NP_001317214.1:n.47-20C>A
NM_016499.6:c.47-20C>A	NP_057583.2:n.47-20C>A