Canonical Allele Identifier: CA1977296934

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393898T= , CM000673.2:g.61393898T=	GRCh38
NC_000011.9:g.61161370T= , CM000673.1:g.61161370T=	GRCh37
NC_000011.8:g.60917946T=	NCBI36
NG_032976.1:g.6539T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.151T=	ENSP00000334844.5:p.Tyr51=
ENST00000544795.6:n.428T=
ENST00000684926.1:n.167T=
ENST00000688959.1:c.-109T=	ENSP00000509213.1:n.-109T=
ENST00000690736.1:c.151T=	ENSP00000508542.1:p.Tyr51=
ENST00000515837.7:c.151T= MANE Select	ENSP00000440638.1:p.Tyr51=
ENST00000334888.9:c.151T=	ENSP00000334844.5:p.Tyr51=
ENST00000398979.7:c.-33T=	ENSP00000381950.3:n.-33T=
ENST00000515837.6:c.151T=	ENSP00000440638.1:p.Tyr51=
ENST00000541473.1:n.165T=
ENST00000544795.5:n.167T=
NM_001173990.2:c.151T=	NP_001167461.1:p.Tyr51=
NM_001173991.2:c.151T=	NP_001167462.1:p.Tyr51=
NM_016499.5:c.-33T=	NP_057583.2:n.-33T=
XM_005274039.3:c.-33T=	XP_005274096.1:n.-33T=
NM_001330285.1:c.-33T=	NP_001317214.1:n.-33T=
XM_005274039.4:c.-33T=	XP_005274096.1:n.-33T=
NM_001173990.3:c.151T= MANE Select	NP_001167461.1:p.Tyr51=
NM_001173991.3:c.151T=	NP_001167462.1:p.Tyr51=
NM_001330285.2:c.-33T=	NP_001317214.1:n.-33T=
NM_016499.6:c.-33T=	NP_057583.2:n.-33T=