Canonical Allele Identifier: CA1977295663

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392591C= , CM000673.2:g.61392591C=	GRCh38
NC_000011.9:g.61160063C= , CM000673.1:g.61160063C=	GRCh37
NC_000011.8:g.60916639C=	NCBI36
NG_032976.1:g.5232C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-41C=	ENSP00000334844.5:n.-41C=
ENST00000544795.6:n.5C=
ENST00000690736.1:c.-41C=	ENSP00000508542.1:n.-41C=
ENST00000515837.7:c.-41C= MANE Select	ENSP00000440638.1:n.-41C=
ENST00000334888.9:c.-41C=	ENSP00000334844.5:n.-41C=
ENST00000398979.7:c.-238C=	ENSP00000381950.3:n.-238C=
ENST00000515837.6:c.-41C=	ENSP00000440638.1:n.-41C=
NM_001173990.2:c.-41C=	NP_001167461.1:n.-41C=
NM_001173991.2:c.-41C=	NP_001167462.1:n.-41C=
NM_016499.5:c.-238C=	NP_057583.2:n.-238C=
XM_005274039.3:c.-372C=	XP_005274096.1:n.-372C=
NM_001330285.1:c.-238C=	NP_001317214.1:n.-238C=
XM_005274039.4:c.-372C=	XP_005274096.1:n.-372C=
NM_001173990.3:c.-41C= MANE Select	NP_001167461.1:n.-41C=
NM_001173991.3:c.-41C=	NP_001167462.1:n.-41C=
NM_001330285.2:c.-238C=	NP_001317214.1:n.-238C=
NM_016499.6:c.-238C=	NP_057583.2:n.-238C=