Canonical Allele Identifier: CA2574840934

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392626C>G , CM000673.2:g.61392626C>G	GRCh38
NC_000011.9:g.61160098C>G , CM000673.1:g.61160098C>G	GRCh37
NC_000011.8:g.60916674C>G	NCBI36
NG_032976.1:g.5267C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-6C>G	ENSP00000334844.5:n.-6C>G
ENST00000544795.6:n.40C>G
ENST00000688959.1:c.-279C>G	ENSP00000509213.1:n.-279C>G
ENST00000690736.1:c.-6C>G	ENSP00000508542.1:n.-6C>G
ENST00000515837.7:c.-6C>G MANE Select	ENSP00000440638.1:n.-6C>G
ENST00000334888.9:c.-6C>G	ENSP00000334844.5:n.-6C>G
ENST00000398979.7:c.-203C>G	ENSP00000381950.3:n.-203C>G
ENST00000515837.6:c.-6C>G	ENSP00000440638.1:n.-6C>G
NM_001173990.2:c.-6C>G	NP_001167461.1:n.-6C>G
NM_001173991.2:c.-6C>G	NP_001167462.1:n.-6C>G
NM_016499.5:c.-203C>G	NP_057583.2:n.-203C>G
XM_005274039.3:c.-337C>G	XP_005274096.1:n.-337C>G
NM_001330285.1:c.-203C>G	NP_001317214.1:n.-203C>G
XM_005274039.4:c.-337C>G	XP_005274096.1:n.-337C>G
NM_001173990.3:c.-6C>G MANE Select	NP_001167461.1:n.-6C>G
NM_001173991.3:c.-6C>G	NP_001167462.1:n.-6C>G
NM_001330285.2:c.-203C>G	NP_001317214.1:n.-203C>G
NM_016499.6:c.-203C>G	NP_057583.2:n.-203C>G