Canonical Allele Identifier: CA1977296199

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393032A= , CM000673.2:g.61393032A=	GRCh38
NC_000011.9:g.61160504A= , CM000673.1:g.61160504A=	GRCh37
NC_000011.8:g.60917080A=	NCBI36
NG_032976.1:g.5673A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.35-199A=	ENSP00000334844.5:n.35-199A=
ENST00000544795.6:n.311+135A=
ENST00000684926.1:n.51-199A=
ENST00000688959.1:c.-225-199A=	ENSP00000509213.1:n.-225-199A=
ENST00000690736.1:c.35-199A=	ENSP00000508542.1:n.35-199A=
ENST00000515837.7:c.35-199A= MANE Select	ENSP00000440638.1:n.35-199A=
ENST00000334888.9:c.35-199A=	ENSP00000334844.5:n.35-199A=
ENST00000398979.7:c.-149-199A=	ENSP00000381950.3:n.-149-199A=
ENST00000515837.6:c.35-199A=	ENSP00000440638.1:n.35-199A=
ENST00000541473.1:n.49-199A=
ENST00000544795.5:n.51-199A=
NM_001173990.2:c.35-199A=	NP_001167461.1:n.35-199A=
NM_001173991.2:c.35-199A=	NP_001167462.1:n.35-199A=
NM_016499.5:c.-149-199A=	NP_057583.2:n.-149-199A=
XM_005274039.3:c.-150+135A=	XP_005274096.1:n.-150+135A=
NM_001330285.1:c.-149-199A=	NP_001317214.1:n.-149-199A=
XM_005274039.4:c.-150+135A=	XP_005274096.1:n.-150+135A=
NM_001173990.3:c.35-199A= MANE Select	NP_001167461.1:n.35-199A=
NM_001173991.3:c.35-199A=	NP_001167462.1:n.35-199A=
NM_001330285.2:c.-149-199A=	NP_001317214.1:n.-149-199A=
NM_016499.6:c.-149-199A=	NP_057583.2:n.-149-199A=