Canonical Allele Identifier: CA380684551

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61393241-G-T
• MyVariant Identifiers: chr11:g.61160713G>T (hg19) ; chr11:g.61393241G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393241G>T , CM000673.2:g.61393241G>T	GRCh38
NC_000011.9:g.61160713G>T , CM000673.1:g.61160713G>T	GRCh37
NC_000011.8:g.60917289G>T	NCBI36
NG_032976.1:g.5882G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.45G>T	ENSP00000334844.5:p.Leu15Phe
ENST00000544795.6:n.322G>T
ENST00000684926.1:n.61G>T
ENST00000688959.1:c.-215G>T	ENSP00000509213.1:n.-215G>T
ENST00000690736.1:c.45G>T	ENSP00000508542.1:p.Leu15Phe
ENST00000515837.7:c.45G>T MANE Select	ENSP00000440638.1:p.Leu15Phe
ENST00000334888.9:c.45G>T	ENSP00000334844.5:p.Leu15Phe
ENST00000398979.7:c.-139G>T	ENSP00000381950.3:n.-139G>T
ENST00000515837.6:c.45G>T	ENSP00000440638.1:p.Leu15Phe
ENST00000541473.1:n.59G>T
ENST00000544795.5:n.61G>T
NM_001173990.2:c.45G>T	NP_001167461.1:p.Leu15Phe
NM_001173991.2:c.45G>T	NP_001167462.1:p.Leu15Phe
NM_016499.5:c.-139G>T	NP_057583.2:n.-139G>T
XM_005274039.3:c.-139G>T	XP_005274096.1:n.-139G>T
NM_001330285.1:c.-139G>T	NP_001317214.1:n.-139G>T
XM_005274039.4:c.-139G>T	XP_005274096.1:n.-139G>T
NM_001173990.3:c.45G>T MANE Select	NP_001167461.1:p.Leu15Phe
NM_001173991.3:c.45G>T	NP_001167462.1:p.Leu15Phe
NM_001330285.2:c.-139G>T	NP_001317214.1:n.-139G>T
NM_016499.6:c.-139G>T	NP_057583.2:n.-139G>T