Canonical Allele Identifier: CA2613837998

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61394072-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61394072C>A , CM000673.2:g.61394072C>A	GRCh38
NC_000011.9:g.61161544C>A , CM000673.1:g.61161544C>A	GRCh37
NC_000011.8:g.60918120C>A	NCBI36
NG_032976.1:g.6713C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.229+96C>A	ENSP00000334844.5:n.229+96C>A
ENST00000544795.6:n.506+96C>A
ENST00000684926.1:n.245+96C>A
ENST00000688959.1:c.-22+87C>A	ENSP00000509213.1:n.-22+87C>A
ENST00000690736.1:c.229+96C>A	ENSP00000508542.1:n.229+96C>A
ENST00000515837.7:c.229+96C>A MANE Select	ENSP00000440638.1:n.229+96C>A
ENST00000334888.9:c.229+96C>A	ENSP00000334844.5:n.229+96C>A
ENST00000398979.7:c.46+96C>A	ENSP00000381950.3:n.46+96C>A
ENST00000515837.6:c.229+96C>A	ENSP00000440638.1:n.229+96C>A
ENST00000541473.1:n.339C>A
ENST00000544795.5:n.245+96C>A
NM_001173990.2:c.229+96C>A	NP_001167461.1:n.229+96C>A
NM_001173991.2:c.229+96C>A	NP_001167462.1:n.229+96C>A
NM_016499.5:c.46+96C>A	NP_057583.2:n.46+96C>A
XM_005274039.3:c.46+96C>A	XP_005274096.1:n.46+96C>A
NM_001330285.1:c.46+96C>A	NP_001317214.1:n.46+96C>A
XM_005274039.4:c.46+96C>A	XP_005274096.1:n.46+96C>A
NM_001173990.3:c.229+96C>A MANE Select	NP_001167461.1:n.229+96C>A
NM_001173991.3:c.229+96C>A	NP_001167462.1:n.229+96C>A
NM_001330285.2:c.46+96C>A	NP_001317214.1:n.46+96C>A
NM_016499.6:c.46+96C>A	NP_057583.2:n.46+96C>A