Canonical Allele Identifier: CA1977296931

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393893T= , CM000673.2:g.61393893T=	GRCh38
NC_000011.9:g.61161365T= , CM000673.1:g.61161365T=	GRCh37
NC_000011.8:g.60917941T=	NCBI36
NG_032976.1:g.6534T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.146T=	ENSP00000334844.5:p.Leu49=
ENST00000544795.6:n.423T=
ENST00000684926.1:n.162T=
ENST00000688959.1:c.-114T=	ENSP00000509213.1:n.-114T=
ENST00000690736.1:c.146T=	ENSP00000508542.1:p.Leu49=
ENST00000515837.7:c.146T= MANE Select	ENSP00000440638.1:p.Leu49=
ENST00000334888.9:c.146T=	ENSP00000334844.5:p.Leu49=
ENST00000398979.7:c.-38T=	ENSP00000381950.3:n.-38T=
ENST00000515837.6:c.146T=	ENSP00000440638.1:p.Leu49=
ENST00000541473.1:n.160T=
ENST00000544795.5:n.162T=
NM_001173990.2:c.146T=	NP_001167461.1:p.Leu49=
NM_001173991.2:c.146T=	NP_001167462.1:p.Leu49=
NM_016499.5:c.-38T=	NP_057583.2:n.-38T=
XM_005274039.3:c.-38T=	XP_005274096.1:n.-38T=
NM_001330285.1:c.-38T=	NP_001317214.1:n.-38T=
XM_005274039.4:c.-38T=	XP_005274096.1:n.-38T=
NM_001173990.3:c.146T= MANE Select	NP_001167461.1:p.Leu49=
NM_001173991.3:c.146T=	NP_001167462.1:p.Leu49=
NM_001330285.2:c.-38T=	NP_001317214.1:n.-38T=
NM_016499.6:c.-38T=	NP_057583.2:n.-38T=