Canonical Allele Identifier: CA2613836067

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392458-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392458C>G , CM000673.2:g.61392458C>G	GRCh38
NC_000011.9:g.61159930C>G , CM000673.1:g.61159930C>G	GRCh37
NC_000011.8:g.60916506C>G	NCBI36
NG_032976.1:g.5099C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-174C>G	ENSP00000334844.5:n.-174C>G
ENST00000398979.7:c.-371C>G	ENSP00000381950.3:n.-371C>G
ENST00000515837.6:c.-174C>G	ENSP00000440638.1:n.-174C>G
NM_001173990.2:c.-174C>G	NP_001167461.1:n.-174C>G
NM_001173991.2:c.-174C>G	NP_001167462.1:n.-174C>G
NM_016499.5:c.-371C>G	NP_057583.2:n.-371C>G
XM_005274039.3:c.-505C>G	XP_005274096.1:n.-505C>G
NM_001330285.1:c.-371C>G	NP_001317214.1:n.-371C>G
XM_005274039.4:c.-505C>G	XP_005274096.1:n.-505C>G