Canonical Allele Identifier: CA1977295518

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392475G= , CM000673.2:g.61392475G=	GRCh38
NC_000011.9:g.61159947G= , CM000673.1:g.61159947G=	GRCh37
NC_000011.8:g.60916523G=	NCBI36
NG_032976.1:g.5116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-157G=	ENSP00000334844.5:n.-157G=
ENST00000398979.7:c.-354G=	ENSP00000381950.3:n.-354G=
ENST00000515837.6:c.-157G=	ENSP00000440638.1:n.-157G=
NM_001173990.2:c.-157G=	NP_001167461.1:n.-157G=
NM_001173991.2:c.-157G=	NP_001167462.1:n.-157G=
NM_016499.5:c.-354G=	NP_057583.2:n.-354G=
XM_005274039.3:c.-488G=	XP_005274096.1:n.-488G=
NM_001330285.1:c.-354G=	NP_001317214.1:n.-354G=
XM_005274039.4:c.-488G=	XP_005274096.1:n.-488G=