Canonical Allele Identifier: CA1977295825

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392654T= , CM000673.2:g.61392654T=	GRCh38
NC_000011.9:g.61160126T= , CM000673.1:g.61160126T=	GRCh37
NC_000011.8:g.60916702T=	NCBI36
NG_032976.1:g.5295T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.23T=	ENSP00000334844.5:p.Met8=
ENST00000544795.6:n.68T=
ENST00000684926.1:n.25T=
ENST00000688959.1:c.-251T=	ENSP00000509213.1:n.-251T=
ENST00000690736.1:c.23T=	ENSP00000508542.1:p.Met8=
ENST00000515837.7:c.23T= MANE Select	ENSP00000440638.1:p.Met8=
ENST00000334888.9:c.23T=	ENSP00000334844.5:p.Met8=
ENST00000398979.7:c.-175T=	ENSP00000381950.3:n.-175T=
ENST00000515837.6:c.23T=	ENSP00000440638.1:p.Met8=
ENST00000541473.1:n.23T=
ENST00000544795.5:n.25T=
NM_001173990.2:c.23T=	NP_001167461.1:p.Met8=
NM_001173991.2:c.23T=	NP_001167462.1:p.Met8=
NM_016499.5:c.-175T=	NP_057583.2:n.-175T=
XM_005274039.3:c.-309T=	XP_005274096.1:n.-309T=
NM_001330285.1:c.-175T=	NP_001317214.1:n.-175T=
XM_005274039.4:c.-309T=	XP_005274096.1:n.-309T=
NM_001173990.3:c.23T= MANE Select	NP_001167461.1:p.Met8=
NM_001173991.3:c.23T=	NP_001167462.1:p.Met8=
NM_001330285.2:c.-175T=	NP_001317214.1:n.-175T=
NM_016499.6:c.-175T=	NP_057583.2:n.-175T=