Canonical Allele Identifier: CA1977297080

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393971T= , CM000673.2:g.61393971T=	GRCh38
NC_000011.9:g.61161443T= , CM000673.1:g.61161443T=	GRCh37
NC_000011.8:g.60918019T=	NCBI36
NG_032976.1:g.6612T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.224T=	ENSP00000334844.5:p.Phe75=
ENST00000544795.6:n.501T=
ENST00000684926.1:n.240T=
ENST00000688959.1:c.-36T=	ENSP00000509213.1:n.-36T=
ENST00000690736.1:c.224T=	ENSP00000508542.1:p.Phe75=
ENST00000515837.7:c.224T= MANE Select	ENSP00000440638.1:p.Phe75=
ENST00000334888.9:c.224T=	ENSP00000334844.5:p.Phe75=
ENST00000398979.7:c.41T=	ENSP00000381950.3:p.Phe14=
ENST00000515837.6:c.224T=	ENSP00000440638.1:p.Phe75=
ENST00000541473.1:n.238T=
ENST00000544795.5:n.240T=
NM_001173990.2:c.224T=	NP_001167461.1:p.Phe75=
NM_001173991.2:c.224T=	NP_001167462.1:p.Phe75=
NM_016499.5:c.41T=	NP_057583.2:p.Phe14=
XM_005274039.3:c.41T=	XP_005274096.1:p.Phe14=
NM_001330285.1:c.41T=	NP_001317214.1:p.Phe14=
XM_005274039.4:c.41T=	XP_005274096.1:p.Phe14=
NM_001173990.3:c.224T= MANE Select	NP_001167461.1:p.Phe75=
NM_001173991.3:c.224T=	NP_001167462.1:p.Phe75=
NM_001330285.2:c.41T=	NP_001317214.1:p.Phe14=
NM_016499.6:c.41T=	NP_057583.2:p.Phe14=