Canonical Allele Identifier: CA912972742

Gene: TMEM216

Linked Data

• MyVariant Identifiers: chr11:g.61160151_61160155del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392680_61392684del , CM000673.2:g.61392680_61392684del	GRCh38
NC_000011.9:g.61160152_61160156del , CM000673.1:g.61160152_61160156del	GRCh37
NC_000011.8:g.60916728_60916732del	NCBI36
NG_032976.1:g.5321_5325del

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.34+15_34+19del	ENSP00000334844.5:n.34+15_34+19del
ENST00000544795.6:n.94_98del
ENST00000684926.1:n.50+1_50+5del
ENST00000688959.1:c.-226+1_-226+5del
ENST00000690736.1:c.34+15_34+19del	ENSP00000508542.1:n.34+15_34+19del
ENST00000515837.7:c.34+15_34+19del MANE Select	ENSP00000440638.1:n.34+15_34+19del
ENST00000334888.9:c.34+15_34+19del	ENSP00000334844.5:n.34+15_34+19del
ENST00000398979.7:c.-150+1_-150+5del
ENST00000515837.6:c.34+15_34+19del	ENSP00000440638.1:n.34+15_34+19del
ENST00000541473.1:n.48+1_48+5del
ENST00000544795.5:n.50+1_50+5del
NM_001173990.2:c.34+15_34+19del	NP_001167461.1:n.34+15_34+19del
NM_001173991.2:c.34+15_34+19del	NP_001167462.1:n.34+15_34+19del
NM_016499.5:c.-150+1_-150+5del
XM_005274039.3:c.-284+1_-284+5del
NM_001330285.1:c.-150+1_-150+5del
XM_005274039.4:c.-284+1_-284+5del
NM_001173990.3:c.34+15_34+19del MANE Select	NP_001167461.1:n.34+15_34+19del
NM_001173991.3:c.34+15_34+19del	NP_001167462.1:n.34+15_34+19del
NM_001330285.2:c.-150+1_-150+5del
NM_016499.6:c.-150+1_-150+5del