Canonical Allele Identifier: CA1977295631

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392563G= , CM000673.2:g.61392563G=	GRCh38
NC_000011.9:g.61160035G= , CM000673.1:g.61160035G=	GRCh37
NC_000011.8:g.60916611G=	NCBI36
NG_032976.1:g.5204G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-69G=	ENSP00000334844.5:n.-69G=
ENST00000398979.7:c.-266G=	ENSP00000381950.3:n.-266G=
ENST00000515837.6:c.-69G=	ENSP00000440638.1:n.-69G=
NM_001173990.2:c.-69G=	NP_001167461.1:n.-69G=
NM_001173991.2:c.-69G=	NP_001167462.1:n.-69G=
NM_016499.5:c.-266G=	NP_057583.2:n.-266G=
XM_005274039.3:c.-400G=	XP_005274096.1:n.-400G=
NM_001330285.1:c.-266G=	NP_001317214.1:n.-266G=
XM_005274039.4:c.-400G=	XP_005274096.1:n.-400G=