Canonical Allele Identifier: CA1977295675

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392601C= , CM000673.2:g.61392601C=	GRCh38
NC_000011.9:g.61160073C= , CM000673.1:g.61160073C=	GRCh37
NC_000011.8:g.60916649C=	NCBI36
NG_032976.1:g.5242C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-31C=	ENSP00000334844.5:n.-31C=
ENST00000544795.6:n.15C=
ENST00000690736.1:c.-31C=	ENSP00000508542.1:n.-31C=
ENST00000515837.7:c.-31C= MANE Select	ENSP00000440638.1:n.-31C=
ENST00000334888.9:c.-31C=	ENSP00000334844.5:n.-31C=
ENST00000398979.7:c.-228C=	ENSP00000381950.3:n.-228C=
ENST00000515837.6:c.-31C=	ENSP00000440638.1:n.-31C=
NM_001173990.2:c.-31C=	NP_001167461.1:n.-31C=
NM_001173991.2:c.-31C=	NP_001167462.1:n.-31C=
NM_016499.5:c.-228C=	NP_057583.2:n.-228C=
XM_005274039.3:c.-362C=	XP_005274096.1:n.-362C=
NM_001330285.1:c.-228C=	NP_001317214.1:n.-228C=
XM_005274039.4:c.-362C=	XP_005274096.1:n.-362C=
NM_001173990.3:c.-31C= MANE Select	NP_001167461.1:n.-31C=
NM_001173991.3:c.-31C=	NP_001167462.1:n.-31C=
NM_001330285.2:c.-228C=	NP_001317214.1:n.-228C=
NM_016499.6:c.-228C=	NP_057583.2:n.-228C=