Canonical Allele Identifier: CA1977295465

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392403C= , CM000673.2:g.61392403C=	GRCh38
NC_000011.9:g.61159875C= , CM000673.1:g.61159875C=	GRCh37
NC_000011.8:g.60916451C=	NCBI36
NG_032976.1:g.5044C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-229C=	ENSP00000334844.5:n.-229C=
ENST00000398979.7:c.-426C=	ENSP00000381950.3:n.-426C=
ENST00000515837.6:c.-229C=	ENSP00000440638.1:n.-229C=
NM_001173990.2:c.-229C=	NP_001167461.1:n.-229C=
NM_001173991.2:c.-229C=	NP_001167462.1:n.-229C=
NM_016499.5:c.-426C=	NP_057583.2:n.-426C=
XM_005274039.3:c.-560C=	XP_005274096.1:n.-560C=
NM_001330285.1:c.-426C=	NP_001317214.1:n.-426C=
XM_005274039.4:c.-560C=	XP_005274096.1:n.-560C=