Canonical Allele Identifier: CA2574840937

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392631-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392631T>G , CM000673.2:g.61392631T>G	GRCh38
NC_000011.9:g.61160103T>G , CM000673.1:g.61160103T>G	GRCh37
NC_000011.8:g.60916679T>G	NCBI36
NG_032976.1:g.5272T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-1T>G	ENSP00000334844.5:n.-1T>G
ENST00000544795.6:n.45T>G
ENST00000684926.1:n.2T>G
ENST00000688959.1:c.-274T>G	ENSP00000509213.1:n.-274T>G
ENST00000690736.1:c.-1T>G	ENSP00000508542.1:n.-1T>G
ENST00000515837.7:c.-1T>G MANE Select	ENSP00000440638.1:n.-1T>G
ENST00000334888.9:c.-1T>G	ENSP00000334844.5:n.-1T>G
ENST00000398979.7:c.-198T>G	ENSP00000381950.3:n.-198T>G
ENST00000515837.6:c.-1T>G	ENSP00000440638.1:n.-1T>G
ENST00000544795.5:n.2T>G
NM_001173990.2:c.-1T>G	NP_001167461.1:n.-1T>G
NM_001173991.2:c.-1T>G	NP_001167462.1:n.-1T>G
NM_016499.5:c.-198T>G	NP_057583.2:n.-198T>G
XM_005274039.3:c.-332T>G	XP_005274096.1:n.-332T>G
NM_001330285.1:c.-198T>G	NP_001317214.1:n.-198T>G
XM_005274039.4:c.-332T>G	XP_005274096.1:n.-332T>G
NM_001173990.3:c.-1T>G MANE Select	NP_001167461.1:n.-1T>G
NM_001173991.3:c.-1T>G	NP_001167462.1:n.-1T>G
NM_001330285.2:c.-198T>G	NP_001317214.1:n.-198T>G
NM_016499.6:c.-198T>G	NP_057583.2:n.-198T>G