Canonical Allele Identifier: CA474518942

Gene: TMEM216

Linked Data

• MyVariant Identifiers: chr11:g.61161378A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393906A>G , CM000673.2:g.61393906A>G	GRCh38
NC_000011.9:g.61161378A>G , CM000673.1:g.61161378A>G	GRCh37
NC_000011.8:g.60917954A>G	NCBI36
NG_032976.1:g.6547A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.159A>G	ENSP00000334844.5:p.Thr53=
ENST00000544795.6:n.436A>G
ENST00000684926.1:n.175A>G
ENST00000688959.1:c.-101A>G	ENSP00000509213.1:n.-101A>G
ENST00000690736.1:c.159A>G	ENSP00000508542.1:p.Thr53=
ENST00000515837.7:c.159A>G MANE Select	ENSP00000440638.1:p.Thr53=
ENST00000334888.9:c.159A>G	ENSP00000334844.5:p.Thr53=
ENST00000398979.7:c.-25A>G	ENSP00000381950.3:n.-25A>G
ENST00000515837.6:c.159A>G	ENSP00000440638.1:p.Thr53=
ENST00000541473.1:n.173A>G
ENST00000544795.5:n.175A>G
NM_001173990.2:c.159A>G	NP_001167461.1:p.Thr53=
NM_001173991.2:c.159A>G	NP_001167462.1:p.Thr53=
NM_016499.5:c.-25A>G	NP_057583.2:n.-25A>G
XM_005274039.3:c.-25A>G	XP_005274096.1:n.-25A>G
NM_001330285.1:c.-25A>G	NP_001317214.1:n.-25A>G
XM_005274039.4:c.-25A>G	XP_005274096.1:n.-25A>G
NM_001173990.3:c.159A>G MANE Select	NP_001167461.1:p.Thr53=
NM_001173991.3:c.159A>G	NP_001167462.1:p.Thr53=
NM_001330285.2:c.-25A>G	NP_001317214.1:n.-25A>G
NM_016499.6:c.-25A>G	NP_057583.2:n.-25A>G