Canonical Allele Identifier: CA6034697

Gene: TMEM216

Linked Data

• ClinVar Variation Id: 857506
• ClinVar RCV Id: RCV001833617
• dbSNP Id: rs528271337
• ExAC: 11:61160708 C / T
• gnomAD v2: 11-61160708-C-T
• gnomAD v3: 11-61393236-C-T
• gnomAD v4: 11-61393236-C-T
• MyVariant Identifiers: chr11:g.61160708C>T (hg19) ; chr11:g.61393236C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393236C>T , CM000673.2:g.61393236C>T	GRCh38
NC_000011.9:g.61160708C>T , CM000673.1:g.61160708C>T	GRCh37
NC_000011.8:g.60917284C>T	NCBI36
NG_032976.1:g.5877C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.40C>T	ENSP00000334844.5:p.Arg14Trp
ENST00000544795.6:n.317C>T
ENST00000684926.1:n.56C>T
ENST00000688959.1:c.-220C>T	ENSP00000509213.1:n.-220C>T
ENST00000690736.1:c.40C>T	ENSP00000508542.1:p.Arg14Trp
ENST00000515837.7:c.40C>T MANE Select	ENSP00000440638.1:p.Arg14Trp
ENST00000334888.9:c.40C>T	ENSP00000334844.5:p.Arg14Trp
ENST00000398979.7:c.-144C>T	ENSP00000381950.3:n.-144C>T
ENST00000515837.6:c.40C>T	ENSP00000440638.1:p.Arg14Trp
ENST00000541473.1:n.54C>T
ENST00000544795.5:n.56C>T
NM_001173990.2:c.40C>T	NP_001167461.1:p.Arg14Trp
NM_001173991.2:c.40C>T	NP_001167462.1:p.Arg14Trp
NM_016499.5:c.-144C>T	NP_057583.2:n.-144C>T
XM_005274039.3:c.-144C>T	XP_005274096.1:n.-144C>T
NM_001330285.1:c.-144C>T	NP_001317214.1:n.-144C>T
XM_005274039.4:c.-144C>T	XP_005274096.1:n.-144C>T
NM_001173990.3:c.40C>T MANE Select	NP_001167461.1:p.Arg14Trp
NM_001173991.3:c.40C>T	NP_001167462.1:p.Arg14Trp
NM_001330285.2:c.-144C>T	NP_001317214.1:n.-144C>T
NM_016499.6:c.-144C>T	NP_057583.2:n.-144C>T