Canonical Allele Identifier: CA2613837851

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61393989-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393990del , CM000673.2:g.61393990del	GRCh38
NC_000011.9:g.61161462del , CM000673.1:g.61161462del	GRCh37
NC_000011.8:g.60918038del	NCBI36
NG_032976.1:g.6631del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.229+14del	ENSP00000334844.5:n.229+14del
ENST00000544795.6:n.506+14del
ENST00000684926.1:n.245+14del
ENST00000688959.1:c.-22+5del	ENSP00000509213.1:n.-22+5del
ENST00000690736.1:c.229+14del	ENSP00000508542.1:n.229+14del
ENST00000515837.7:c.229+14del MANE Select	ENSP00000440638.1:n.229+14del
ENST00000334888.9:c.229+14del	ENSP00000334844.5:n.229+14del
ENST00000398979.7:c.46+14del	ENSP00000381950.3:n.46+14del
ENST00000515837.6:c.229+14del	ENSP00000440638.1:n.229+14del
ENST00000541473.1:n.257del
ENST00000544795.5:n.245+14del
NM_001173990.2:c.229+14del	NP_001167461.1:n.229+14del
NM_001173991.2:c.229+14del	NP_001167462.1:n.229+14del
NM_016499.5:c.46+14del	NP_057583.2:n.46+14del
XM_005274039.3:c.46+14del	XP_005274096.1:n.46+14del
NM_001330285.1:c.46+14del	NP_001317214.1:n.46+14del
XM_005274039.4:c.46+14del	XP_005274096.1:n.46+14del
NM_001173990.3:c.229+14del MANE Select	NP_001167461.1:n.229+14del
NM_001173991.3:c.229+14del	NP_001167462.1:n.229+14del
NM_001330285.2:c.46+14del	NP_001317214.1:n.46+14del
NM_016499.6:c.46+14del	NP_057583.2:n.46+14del