Canonical Allele Identifier: CA912972745

Gene: TMEM216

Linked Data

• MyVariant Identifiers: chr11:g.61165236dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397764dup , CM000673.2:g.61397764dup	GRCh38
NC_000011.9:g.61165236dup , CM000673.1:g.61165236dup	GRCh37
NC_000011.8:g.60921812dup	NCBI36
NG_032976.1:g.10405dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.230-10dup	ENSP00000334844.5:n.230-10dup
ENST00000544795.6:n.543dup
ENST00000684926.1:n.282dup
ENST00000688959.1:c.-21-18dup	ENSP00000509213.1:n.-21-18dup
ENST00000690736.1:c.266dup	ENSP00000508542.1:p.Ser90ValfsTer2
ENST00000515837.7:c.230-10dup MANE Select	ENSP00000440638.1:n.230-10dup
ENST00000334888.9:c.230-10dup	ENSP00000334844.5:n.230-10dup
ENST00000398979.7:c.47-10dup	ENSP00000381950.3:n.47-10dup
ENST00000515837.6:c.230-10dup	ENSP00000440638.1:n.230-10dup
ENST00000544795.5:n.282dup
NM_001173990.2:c.230-10dup	NP_001167461.1:n.230-10dup
NM_001173991.2:c.230-10dup	NP_001167462.1:n.230-10dup
NM_016499.5:c.47-10dup	NP_057583.2:n.47-10dup
XM_005274039.3:c.47-10dup	XP_005274096.1:n.47-10dup
NM_001330285.1:c.47-10dup	NP_001317214.1:n.47-10dup
XM_005274039.4:c.47-10dup	XP_005274096.1:n.47-10dup
NM_001173990.3:c.230-10dup MANE Select	NP_001167461.1:n.230-10dup
NM_001173991.3:c.230-10dup	NP_001167462.1:n.230-10dup
NM_001330285.2:c.47-10dup	NP_001317214.1:n.47-10dup
NM_016499.6:c.47-10dup	NP_057583.2:n.47-10dup