Canonical Allele Identifier: CA1977300091

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397806C= , CM000673.2:g.61397806C=	GRCh38
NC_000011.9:g.61165278C= , CM000673.1:g.61165278C=	GRCh37
NC_000011.8:g.60921854C=	NCBI36
NG_032976.1:g.10447C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.262C=	ENSP00000334844.5:p.Pro88=
ENST00000544795.6:n.585C=
ENST00000684926.1:n.324C=
ENST00000688959.1:c.4C=	ENSP00000509213.1:p.Pro2=
ENST00000690736.1:c.308C=	ENSP00000508542.1:p.Ala103=
ENST00000515837.7:c.262C= MANE Select	ENSP00000440638.1:p.Pro88=
ENST00000334888.9:c.262C=	ENSP00000334844.5:p.Pro88=
ENST00000398979.7:c.79C=	ENSP00000381950.3:p.Pro27=
ENST00000515837.6:c.262C=	ENSP00000440638.1:p.Pro88=
ENST00000544795.5:n.324C=
NM_001173990.2:c.262C=	NP_001167461.1:p.Pro88=
NM_001173991.2:c.262C=	NP_001167462.1:p.Pro88=
NM_016499.5:c.79C=	NP_057583.2:p.Pro27=
XM_005274039.3:c.79C=	XP_005274096.1:p.Pro27=
NM_001330285.1:c.79C=	NP_001317214.1:p.Pro27=
XM_005274039.4:c.79C=	XP_005274096.1:p.Pro27=
NM_001173990.3:c.262C= MANE Select	NP_001167461.1:p.Pro88=
NM_001173991.3:c.262C=	NP_001167462.1:p.Pro88=
NM_001330285.2:c.79C=	NP_001317214.1:p.Pro27=
NM_016499.6:c.79C=	NP_057583.2:p.Pro27=