Canonical Allele Identifier: CA1977296976

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393929T= , CM000673.2:g.61393929T=	GRCh38
NC_000011.9:g.61161401T= , CM000673.1:g.61161401T=	GRCh37
NC_000011.8:g.60917977T=	NCBI36
NG_032976.1:g.6570T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.182T=	ENSP00000334844.5:p.Val61=
ENST00000544795.6:n.459T=
ENST00000684926.1:n.198T=
ENST00000688959.1:c.-78T=	ENSP00000509213.1:n.-78T=
ENST00000690736.1:c.182T=	ENSP00000508542.1:p.Val61=
ENST00000515837.7:c.182T= MANE Select	ENSP00000440638.1:p.Val61=
ENST00000334888.9:c.182T=	ENSP00000334844.5:p.Val61=
ENST00000398979.7:c.-2T=	ENSP00000381950.3:n.-2T=
ENST00000515837.6:c.182T=	ENSP00000440638.1:p.Val61=
ENST00000541473.1:n.196T=
ENST00000544795.5:n.198T=
NM_001173990.2:c.182T=	NP_001167461.1:p.Val61=
NM_001173991.2:c.182T=	NP_001167462.1:p.Val61=
NM_016499.5:c.-2T=	NP_057583.2:n.-2T=
XM_005274039.3:c.-2T=	XP_005274096.1:n.-2T=
NM_001330285.1:c.-2T=	NP_001317214.1:n.-2T=
XM_005274039.4:c.-2T=	XP_005274096.1:n.-2T=
NM_001173990.3:c.182T= MANE Select	NP_001167461.1:p.Val61=
NM_001173991.3:c.182T=	NP_001167462.1:p.Val61=
NM_001330285.2:c.-2T=	NP_001317214.1:n.-2T=
NM_016499.6:c.-2T=	NP_057583.2:n.-2T=