Canonical Allele Identifier: CA10631070

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61398834G>A , CM000673.2:g.61398834G>A	GRCh38
NC_000011.9:g.61166306G>A , CM000673.1:g.61166306G>A	GRCh37
NC_000011.8:g.60922882G>A	NCBI36
NG_032976.1:g.11476G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.*558G>A	ENSP00000334844.5:n.*558G>A
ENST00000544795.6:n.1319G>A
ENST00000684926.1:n.1058G>A
ENST00000690736.1:c.*721G>A	ENSP00000508542.1:n.*721G>A
ENST00000515837.7:c.*558G>A MANE Select	ENSP00000440638.1:n.*558G>A
ENST00000334888.9:c.*558G>A	ENSP00000334844.5:n.*558G>A
ENST00000515837.6:c.*558G>A	ENSP00000440638.1:n.*558G>A
NM_001173990.2:c.*558G>A	NP_001167461.1:n.*558G>A
NM_001173991.2:c.*558G>A	NP_001167462.1:n.*558G>A
NM_016499.5:c.*558G>A	NP_057583.2:n.*558G>A
XM_005274039.3:c.*558G>A	XP_005274096.1:n.*558G>A
NM_001330285.1:c.*558G>A	NP_001317214.1:n.*558G>A
XM_005274039.4:c.*558G>A	XP_005274096.1:n.*558G>A
NM_001173990.3:c.*558G>A MANE Select	NP_001167461.1:n.*558G>A
NM_001173991.3:c.*558G>A	NP_001167462.1:n.*558G>A
NM_001330285.2:c.*558G>A	NP_001317214.1:n.*558G>A
NM_016499.6:c.*558G>A	NP_057583.2:n.*558G>A