Canonical Allele Identifier: CA1977295458

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392394C= , CM000673.2:g.61392394C=	GRCh38
NC_000011.9:g.61159866C= , CM000673.1:g.61159866C=	GRCh37
NC_000011.8:g.60916442C=	NCBI36
NG_032976.1:g.5035C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-238C=	ENSP00000334844.5:n.-238C=
ENST00000398979.7:c.-435C=	ENSP00000381950.3:n.-435C=
ENST00000515837.6:c.-238C=	ENSP00000440638.1:n.-238C=
NM_001173990.2:c.-238C=	NP_001167461.1:n.-238C=
NM_001173991.2:c.-238C=	NP_001167462.1:n.-238C=
NM_016499.5:c.-435C=	NP_057583.2:n.-435C=
XM_005274039.3:c.-569C=	XP_005274096.1:n.-569C=
NM_001330285.1:c.-435C=	NP_001317214.1:n.-435C=
XM_005274039.4:c.-569C=	XP_005274096.1:n.-569C=