Canonical Allele Identifier: CA1977295537

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858692632

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392491_61392495del , CM000673.2:g.61392491_61392495del	GRCh38
NC_000011.9:g.61159963_61159967del , CM000673.1:g.61159963_61159967del	GRCh37
NC_000011.8:g.60916539_60916543del	NCBI36
NG_032976.1:g.5132_5136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-141_-137del	ENSP00000334844.5:n.-141_-137del
ENST00000398979.7:c.-338_-334del	ENSP00000381950.3:n.-338_-334del
ENST00000515837.6:c.-141_-137del	ENSP00000440638.1:n.-141_-137del
NM_001173990.2:c.-141_-137del	NP_001167461.1:n.-141_-137del
NM_001173991.2:c.-141_-137del	NP_001167462.1:n.-141_-137del
NM_016499.5:c.-338_-334del	NP_057583.2:n.-338_-334del
XM_005274039.3:c.-472_-468del	XP_005274096.1:n.-472_-468del
NM_001330285.1:c.-338_-334del	NP_001317214.1:n.-338_-334del
XM_005274039.4:c.-472_-468del	XP_005274096.1:n.-472_-468del