Canonical Allele Identifier: CA2613836258

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392516-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392516G>T , CM000673.2:g.61392516G>T	GRCh38
NC_000011.9:g.61159988G>T , CM000673.1:g.61159988G>T	GRCh37
NC_000011.8:g.60916564G>T	NCBI36
NG_032976.1:g.5157G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-116G>T	ENSP00000334844.5:n.-116G>T
ENST00000398979.7:c.-313G>T	ENSP00000381950.3:n.-313G>T
ENST00000515837.6:c.-116G>T	ENSP00000440638.1:n.-116G>T
NM_001173990.2:c.-116G>T	NP_001167461.1:n.-116G>T
NM_001173991.2:c.-116G>T	NP_001167462.1:n.-116G>T
NM_016499.5:c.-313G>T	NP_057583.2:n.-313G>T
XM_005274039.3:c.-447G>T	XP_005274096.1:n.-447G>T
NM_001330285.1:c.-313G>T	NP_001317214.1:n.-313G>T
XM_005274039.4:c.-447G>T	XP_005274096.1:n.-447G>T