Canonical Allele Identifier: CA1977295669

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392596_61392606delinsAGCGCCGCGCT , CM000673.2:g.61392596_61392606delinsAGCGCCGCGCT	GRCh38
NC_000011.9:g.61160068_61160078delinsAGCGCCGCGCT , CM000673.1:g.61160068_61160078delinsAGCGCCGCGCT	GRCh37
NC_000011.8:g.60916644_60916654delinsAGCGCCGCGCT	NCBI36
NG_032976.1:g.5237_5247delinsAGCGCCGCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-36_-26delinsAGCGCCGCGCT	ENSP00000334844.5:n.-36_-26delinsAGCGCCGCGCT
ENST00000544795.6:n.10_20delinsAGCGCCGCGCT
ENST00000690736.1:c.-36_-26delinsAGCGCCGCGCT	ENSP00000508542.1:n.-36_-26delinsAGCGCCGCGCT
ENST00000515837.7:c.-36_-26delinsAGCGCCGCGCT MANE Select	ENSP00000440638.1:n.-36_-26delinsAGCGCCGCGCT
ENST00000334888.9:c.-36_-26delinsAGCGCCGCGCT	ENSP00000334844.5:n.-36_-26delinsAGCGCCGCGCT
ENST00000398979.7:c.-233_-223delinsAGCGCCGCGCT	ENSP00000381950.3:n.-233_-223delinsAGCGCCGCGCT
ENST00000515837.6:c.-36_-26delinsAGCGCCGCGCT	ENSP00000440638.1:n.-36_-26delinsAGCGCCGCGCT
NM_001173990.2:c.-36_-26delinsAGCGCCGCGCT	NP_001167461.1:n.-36_-26delinsAGCGCCGCGCT
NM_001173991.2:c.-36_-26delinsAGCGCCGCGCT	NP_001167462.1:n.-36_-26delinsAGCGCCGCGCT
NM_016499.5:c.-233_-223delinsAGCGCCGCGCT	NP_057583.2:n.-233_-223delinsAGCGCCGCGCT
XM_005274039.3:c.-367_-357delinsAGCGCCGCGCT	XP_005274096.1:n.-367_-357delinsAGCGCCGCGCT
NM_001330285.1:c.-233_-223delinsAGCGCCGCGCT	NP_001317214.1:n.-233_-223delinsAGCGCCGCGCT
XM_005274039.4:c.-367_-357delinsAGCGCCGCGCT	XP_005274096.1:n.-367_-357delinsAGCGCCGCGCT
NM_001173990.3:c.-36_-26delinsAGCGCCGCGCT MANE Select	NP_001167461.1:n.-36_-26delinsAGCGCCGCGCT
NM_001173991.3:c.-36_-26delinsAGCGCCGCGCT	NP_001167462.1:n.-36_-26delinsAGCGCCGCGCT
NM_001330285.2:c.-233_-223delinsAGCGCCGCGCT	NP_001317214.1:n.-233_-223delinsAGCGCCGCGCT
NM_016499.6:c.-233_-223delinsAGCGCCGCGCT	NP_057583.2:n.-233_-223delinsAGCGCCGCGCT