Canonical Allele Identifier: CA678971536

Gene: TMEM216

Linked Data

• dbSNP Id: rs1449055180
• MyVariant Identifiers: chr11:g.61160005_61160006del (hg19) ; chr11:g.61392533_61392534del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392535_61392536del , CM000673.2:g.61392535_61392536del	GRCh38
NC_000011.9:g.61160007_61160008del , CM000673.1:g.61160007_61160008del	GRCh37
NC_000011.8:g.60916583_60916584del	NCBI36
NG_032976.1:g.5176_5177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-97_-96del	ENSP00000334844.5:n.-97_-96del
ENST00000398979.7:c.-294_-293del	ENSP00000381950.3:n.-294_-293del
ENST00000515837.6:c.-97_-96del	ENSP00000440638.1:n.-97_-96del
NM_001173990.2:c.-97_-96del	NP_001167461.1:n.-97_-96del
NM_001173991.2:c.-97_-96del	NP_001167462.1:n.-97_-96del
NM_016499.5:c.-294_-293del	NP_057583.2:n.-294_-293del
XM_005274039.3:c.-428_-427del	XP_005274096.1:n.-428_-427del
NM_001330285.1:c.-294_-293del	NP_001317214.1:n.-294_-293del
XM_005274039.4:c.-428_-427del	XP_005274096.1:n.-428_-427del