Canonical Allele Identifier: CA1977297030

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393963T= , CM000673.2:g.61393963T=	GRCh38
NC_000011.9:g.61161435T= , CM000673.1:g.61161435T=	GRCh37
NC_000011.8:g.60918011T=	NCBI36
NG_032976.1:g.6604T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.216T=	ENSP00000334844.5:p.Ile72=
ENST00000544795.6:n.493T=
ENST00000684926.1:n.232T=
ENST00000688959.1:c.-44T=	ENSP00000509213.1:n.-44T=
ENST00000690736.1:c.216T=	ENSP00000508542.1:p.Ile72=
ENST00000515837.7:c.216T= MANE Select	ENSP00000440638.1:p.Ile72=
ENST00000334888.9:c.216T=	ENSP00000334844.5:p.Ile72=
ENST00000398979.7:c.33T=	ENSP00000381950.3:p.Ile11=
ENST00000515837.6:c.216T=	ENSP00000440638.1:p.Ile72=
ENST00000541473.1:n.230T=
ENST00000544795.5:n.232T=
NM_001173990.2:c.216T=	NP_001167461.1:p.Ile72=
NM_001173991.2:c.216T=	NP_001167462.1:p.Ile72=
NM_016499.5:c.33T=	NP_057583.2:p.Ile11=
XM_005274039.3:c.33T=	XP_005274096.1:p.Ile11=
NM_001330285.1:c.33T=	NP_001317214.1:p.Ile11=
XM_005274039.4:c.33T=	XP_005274096.1:p.Ile11=
NM_001173990.3:c.216T= MANE Select	NP_001167461.1:p.Ile72=
NM_001173991.3:c.216T=	NP_001167462.1:p.Ile72=
NM_001330285.2:c.33T=	NP_001317214.1:p.Ile11=
NM_016499.6:c.33T=	NP_057583.2:p.Ile11=