Canonical Allele Identifier: CA938603996

Gene: TMEM216

Linked Data

• dbSNP Id: rs1858690764
• gnomAD v3: 11-61392381-GTCTGAGAGCC-G
• gnomAD v4: 11-61392381-GTCTGAGAGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392384_61392393del , CM000673.2:g.61392384_61392393del	GRCh38
NC_000011.9:g.61159856_61159865del , CM000673.1:g.61159856_61159865del	GRCh37
NC_000011.8:g.60916432_60916441del	NCBI36
NG_032976.1:g.5025_5034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-248_-239del	ENSP00000334844.5:n.-248_-239del
ENST00000515837.6:c.-248_-239del	ENSP00000440638.1:n.-248_-239del
NM_001173990.2:c.-248_-239del	NP_001167461.1:n.-248_-239del
NM_001173991.2:c.-248_-239del	NP_001167462.1:n.-248_-239del
XM_005274039.3:c.-579_-570del	XP_005274096.1:n.-579_-570del
NM_001330285.1:c.-445_-436del	NP_001317214.1:n.-445_-436del
XM_005274039.4:c.-579_-570del	XP_005274096.1:n.-579_-570del