Canonical Allele Identifier: CA2613835930

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392401-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392402del , CM000673.2:g.61392402del	GRCh38
NC_000011.9:g.61159874del , CM000673.1:g.61159874del	GRCh37
NC_000011.8:g.60916450del	NCBI36
NG_032976.1:g.5043del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-230del	ENSP00000334844.5:n.-230del
ENST00000398979.7:c.-427del	ENSP00000381950.3:n.-427del
ENST00000515837.6:c.-230del	ENSP00000440638.1:n.-230del
NM_001173990.2:c.-230del	NP_001167461.1:n.-230del
NM_001173991.2:c.-230del	NP_001167462.1:n.-230del
NM_016499.5:c.-427del	NP_057583.2:n.-427del
XM_005274039.3:c.-561del	XP_005274096.1:n.-561del
NM_001330285.1:c.-427del	NP_001317214.1:n.-427del
XM_005274039.4:c.-561del	XP_005274096.1:n.-561del