Canonical Allele Identifier: CA2739270459

Gene: TMEM216

Linked Data

• ClinVar Variation Id: 2831624
• ClinVar RCV Id: RCV003599384

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392675C>G , CM000673.2:g.61392675C>G	GRCh38
NC_000011.9:g.61160147C>G , CM000673.1:g.61160147C>G	GRCh37
NC_000011.8:g.60916723C>G	NCBI36
NG_032976.1:g.5316C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.34+10C>G	ENSP00000334844.5:n.34+10C>G
ENST00000544795.6:n.89C>G
ENST00000684926.1:n.46C>G
ENST00000688959.1:c.-230C>G	ENSP00000509213.1:n.-230C>G
ENST00000690736.1:c.34+10C>G	ENSP00000508542.1:n.34+10C>G
ENST00000515837.7:c.34+10C>G MANE Select	ENSP00000440638.1:n.34+10C>G
ENST00000334888.9:c.34+10C>G	ENSP00000334844.5:n.34+10C>G
ENST00000398979.7:c.-154C>G	ENSP00000381950.3:n.-154C>G
ENST00000515837.6:c.34+10C>G	ENSP00000440638.1:n.34+10C>G
ENST00000541473.1:n.44C>G
ENST00000544795.5:n.46C>G
NM_001173990.2:c.34+10C>G	NP_001167461.1:n.34+10C>G
NM_001173991.2:c.34+10C>G	NP_001167462.1:n.34+10C>G
NM_016499.5:c.-154C>G	NP_057583.2:n.-154C>G
XM_005274039.3:c.-288C>G	XP_005274096.1:n.-288C>G
NM_001330285.1:c.-154C>G	NP_001317214.1:n.-154C>G
XM_005274039.4:c.-288C>G	XP_005274096.1:n.-288C>G
NM_001173990.3:c.34+10C>G MANE Select	NP_001167461.1:n.34+10C>G
NM_001173991.3:c.34+10C>G	NP_001167462.1:n.34+10C>G
NM_001330285.2:c.-154C>G	NP_001317214.1:n.-154C>G
NM_016499.6:c.-154C>G	NP_057583.2:n.-154C>G