Canonical Allele Identifier: CA2613837515

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61393813-TCCCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393814_61393818del , CM000673.2:g.61393814_61393818del	GRCh38
NC_000011.9:g.61161286_61161290del , CM000673.1:g.61161286_61161290del	GRCh37
NC_000011.8:g.60917862_60917866del	NCBI36
NG_032976.1:g.6455_6459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.137-70_137-66del	ENSP00000334844.5:n.137-70_137-66del
ENST00000544795.6:n.414-70_414-66del
ENST00000684926.1:n.153-70_153-66del
ENST00000688959.1:c.-123-70_-123-66del	ENSP00000509213.1:n.-123-70_-123-66del
ENST00000690736.1:c.137-70_137-66del	ENSP00000508542.1:n.137-70_137-66del
ENST00000515837.7:c.137-70_137-66del MANE Select	ENSP00000440638.1:n.137-70_137-66del
ENST00000334888.9:c.137-70_137-66del	ENSP00000334844.5:n.137-70_137-66del
ENST00000398979.7:c.-47-70_-47-66del	ENSP00000381950.3:n.-47-70_-47-66del
ENST00000515837.6:c.137-70_137-66del	ENSP00000440638.1:n.137-70_137-66del
ENST00000541473.1:n.151-70_151-66del
ENST00000544795.5:n.153-70_153-66del
NM_001173990.2:c.137-70_137-66del	NP_001167461.1:n.137-70_137-66del
NM_001173991.2:c.137-70_137-66del	NP_001167462.1:n.137-70_137-66del
NM_016499.5:c.-47-70_-47-66del	NP_057583.2:n.-47-70_-47-66del
XM_005274039.3:c.-47-70_-47-66del	XP_005274096.1:n.-47-70_-47-66del
NM_001330285.1:c.-47-70_-47-66del	NP_001317214.1:n.-47-70_-47-66del
XM_005274039.4:c.-47-70_-47-66del	XP_005274096.1:n.-47-70_-47-66del
NM_001173990.3:c.137-70_137-66del MANE Select	NP_001167461.1:n.137-70_137-66del
NM_001173991.3:c.137-70_137-66del	NP_001167462.1:n.137-70_137-66del
NM_001330285.2:c.-47-70_-47-66del	NP_001317214.1:n.-47-70_-47-66del
NM_016499.6:c.-47-70_-47-66del	NP_057583.2:n.-47-70_-47-66del