Canonical Allele Identifier: CA2613836305

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392546-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392546G>T , CM000673.2:g.61392546G>T	GRCh38
NC_000011.9:g.61160018G>T , CM000673.1:g.61160018G>T	GRCh37
NC_000011.8:g.60916594G>T	NCBI36
NG_032976.1:g.5187G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-86G>T	ENSP00000334844.5:n.-86G>T
ENST00000398979.7:c.-283G>T	ENSP00000381950.3:n.-283G>T
ENST00000515837.6:c.-86G>T	ENSP00000440638.1:n.-86G>T
NM_001173990.2:c.-86G>T	NP_001167461.1:n.-86G>T
NM_001173991.2:c.-86G>T	NP_001167462.1:n.-86G>T
NM_016499.5:c.-283G>T	NP_057583.2:n.-283G>T
XM_005274039.3:c.-417G>T	XP_005274096.1:n.-417G>T
NM_001330285.1:c.-283G>T	NP_001317214.1:n.-283G>T
XM_005274039.4:c.-417G>T	XP_005274096.1:n.-417G>T