Canonical Allele Identifier: CA380685029

Gene: TMEM216

Linked Data

• MyVariant Identifiers: chr11:g.61161364C>A (hg19) ; chr11:g.61393892C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393892C>A , CM000673.2:g.61393892C>A	GRCh38
NC_000011.9:g.61161364C>A , CM000673.1:g.61161364C>A	GRCh37
NC_000011.8:g.60917940C>A	NCBI36
NG_032976.1:g.6533C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.145C>A	ENSP00000334844.5:p.Leu49Ile
ENST00000544795.6:n.422C>A
ENST00000684926.1:n.161C>A
ENST00000688959.1:c.-115C>A	ENSP00000509213.1:n.-115C>A
ENST00000690736.1:c.145C>A	ENSP00000508542.1:p.Leu49Ile
ENST00000515837.7:c.145C>A MANE Select	ENSP00000440638.1:p.Leu49Ile
ENST00000334888.9:c.145C>A	ENSP00000334844.5:p.Leu49Ile
ENST00000398979.7:c.-39C>A	ENSP00000381950.3:n.-39C>A
ENST00000515837.6:c.145C>A	ENSP00000440638.1:p.Leu49Ile
ENST00000541473.1:n.159C>A
ENST00000544795.5:n.161C>A
NM_001173990.2:c.145C>A	NP_001167461.1:p.Leu49Ile
NM_001173991.2:c.145C>A	NP_001167462.1:p.Leu49Ile
NM_016499.5:c.-39C>A	NP_057583.2:n.-39C>A
XM_005274039.3:c.-39C>A	XP_005274096.1:n.-39C>A
NM_001330285.1:c.-39C>A	NP_001317214.1:n.-39C>A
XM_005274039.4:c.-39C>A	XP_005274096.1:n.-39C>A
NM_001173990.3:c.145C>A MANE Select	NP_001167461.1:p.Leu49Ile
NM_001173991.3:c.145C>A	NP_001167462.1:p.Leu49Ile
NM_001330285.2:c.-39C>A	NP_001317214.1:n.-39C>A
NM_016499.6:c.-39C>A	NP_057583.2:n.-39C>A