Canonical Allele Identifier: CA1977295683

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392604G= , CM000673.2:g.61392604G=	GRCh38
NC_000011.9:g.61160076G= , CM000673.1:g.61160076G=	GRCh37
NC_000011.8:g.60916652G=	NCBI36
NG_032976.1:g.5245G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-28G=	ENSP00000334844.5:n.-28G=
ENST00000544795.6:n.18G=
ENST00000690736.1:c.-28G=	ENSP00000508542.1:n.-28G=
ENST00000515837.7:c.-28G= MANE Select	ENSP00000440638.1:n.-28G=
ENST00000334888.9:c.-28G=	ENSP00000334844.5:n.-28G=
ENST00000398979.7:c.-225G=	ENSP00000381950.3:n.-225G=
ENST00000515837.6:c.-28G=	ENSP00000440638.1:n.-28G=
NM_001173990.2:c.-28G=	NP_001167461.1:n.-28G=
NM_001173991.2:c.-28G=	NP_001167462.1:n.-28G=
NM_016499.5:c.-225G=	NP_057583.2:n.-225G=
XM_005274039.3:c.-359G=	XP_005274096.1:n.-359G=
NM_001330285.1:c.-225G=	NP_001317214.1:n.-225G=
XM_005274039.4:c.-359G=	XP_005274096.1:n.-359G=
NM_001173990.3:c.-28G= MANE Select	NP_001167461.1:n.-28G=
NM_001173991.3:c.-28G=	NP_001167462.1:n.-28G=
NM_001330285.2:c.-225G=	NP_001317214.1:n.-225G=
NM_016499.6:c.-225G=	NP_057583.2:n.-225G=