Canonical Allele Identifier: CA2613835915

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392396-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392396A>C , CM000673.2:g.61392396A>C	GRCh38
NC_000011.9:g.61159868A>C , CM000673.1:g.61159868A>C	GRCh37
NC_000011.8:g.60916444A>C	NCBI36
NG_032976.1:g.5037A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-236A>C	ENSP00000334844.5:n.-236A>C
ENST00000398979.7:c.-433A>C	ENSP00000381950.3:n.-433A>C
ENST00000515837.6:c.-236A>C	ENSP00000440638.1:n.-236A>C
NM_001173990.2:c.-236A>C	NP_001167461.1:n.-236A>C
NM_001173991.2:c.-236A>C	NP_001167462.1:n.-236A>C
NM_016499.5:c.-433A>C	NP_057583.2:n.-433A>C
XM_005274039.3:c.-567A>C	XP_005274096.1:n.-567A>C
NM_001330285.1:c.-433A>C	NP_001317214.1:n.-433A>C
XM_005274039.4:c.-567A>C	XP_005274096.1:n.-567A>C