Canonical Allele Identifier: CA2792320017

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392433G>A , CM000673.2:g.61392433G>A	GRCh38
NC_000011.9:g.61159905G>A , CM000673.1:g.61159905G>A	GRCh37
NC_000011.8:g.60916481G>A	NCBI36
NG_032976.1:g.5074G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-199G>A	ENSP00000334844.5:n.-199G>A
ENST00000398979.7:c.-396G>A	ENSP00000381950.3:n.-396G>A
ENST00000515837.6:c.-199G>A	ENSP00000440638.1:n.-199G>A
NM_001173990.2:c.-199G>A	NP_001167461.1:n.-199G>A
NM_001173991.2:c.-199G>A	NP_001167462.1:n.-199G>A
NM_016499.5:c.-396G>A	NP_057583.2:n.-396G>A
XM_005274039.3:c.-530G>A	XP_005274096.1:n.-530G>A
NM_001330285.1:c.-396G>A	NP_001317214.1:n.-396G>A
XM_005274039.4:c.-530G>A	XP_005274096.1:n.-530G>A