Canonical Allele Identifier: CA2613836356

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392594-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392594G>A , CM000673.2:g.61392594G>A	GRCh38
NC_000011.9:g.61160066G>A , CM000673.1:g.61160066G>A	GRCh37
NC_000011.8:g.60916642G>A	NCBI36
NG_032976.1:g.5235G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-38G>A	ENSP00000334844.5:n.-38G>A
ENST00000544795.6:n.8G>A
ENST00000690736.1:c.-38G>A	ENSP00000508542.1:n.-38G>A
ENST00000515837.7:c.-38G>A MANE Select	ENSP00000440638.1:n.-38G>A
ENST00000334888.9:c.-38G>A	ENSP00000334844.5:n.-38G>A
ENST00000398979.7:c.-235G>A	ENSP00000381950.3:n.-235G>A
ENST00000515837.6:c.-38G>A	ENSP00000440638.1:n.-38G>A
NM_001173990.2:c.-38G>A	NP_001167461.1:n.-38G>A
NM_001173991.2:c.-38G>A	NP_001167462.1:n.-38G>A
NM_016499.5:c.-235G>A	NP_057583.2:n.-235G>A
XM_005274039.3:c.-369G>A	XP_005274096.1:n.-369G>A
NM_001330285.1:c.-235G>A	NP_001317214.1:n.-235G>A
XM_005274039.4:c.-369G>A	XP_005274096.1:n.-369G>A
NM_001173990.3:c.-38G>A MANE Select	NP_001167461.1:n.-38G>A
NM_001173991.3:c.-38G>A	NP_001167462.1:n.-38G>A
NM_001330285.2:c.-235G>A	NP_001317214.1:n.-235G>A
NM_016499.6:c.-235G>A	NP_057583.2:n.-235G>A