Canonical Allele Identifier: CA380685050

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61393902-C-T
• MyVariant Identifiers: chr11:g.61161374C>T (hg19) ; chr11:g.61393902C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61393902C>T , CM000673.2:g.61393902C>T	GRCh38
NC_000011.9:g.61161374C>T , CM000673.1:g.61161374C>T	GRCh37
NC_000011.8:g.60917950C>T	NCBI36
NG_032976.1:g.6543C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.155C>T	ENSP00000334844.5:p.Pro52Leu
ENST00000544795.6:n.432C>T
ENST00000684926.1:n.171C>T
ENST00000688959.1:c.-105C>T	ENSP00000509213.1:n.-105C>T
ENST00000690736.1:c.155C>T	ENSP00000508542.1:p.Pro52Leu
ENST00000515837.7:c.155C>T MANE Select	ENSP00000440638.1:p.Pro52Leu
ENST00000334888.9:c.155C>T	ENSP00000334844.5:p.Pro52Leu
ENST00000398979.7:c.-29C>T	ENSP00000381950.3:n.-29C>T
ENST00000515837.6:c.155C>T	ENSP00000440638.1:p.Pro52Leu
ENST00000541473.1:n.169C>T
ENST00000544795.5:n.171C>T
NM_001173990.2:c.155C>T	NP_001167461.1:p.Pro52Leu
NM_001173991.2:c.155C>T	NP_001167462.1:p.Pro52Leu
NM_016499.5:c.-29C>T	NP_057583.2:n.-29C>T
XM_005274039.3:c.-29C>T	XP_005274096.1:n.-29C>T
NM_001330285.1:c.-29C>T	NP_001317214.1:n.-29C>T
XM_005274039.4:c.-29C>T	XP_005274096.1:n.-29C>T
NM_001173990.3:c.155C>T MANE Select	NP_001167461.1:p.Pro52Leu
NM_001173991.3:c.155C>T	NP_001167462.1:p.Pro52Leu
NM_001330285.2:c.-29C>T	NP_001317214.1:n.-29C>T
NM_016499.6:c.-29C>T	NP_057583.2:n.-29C>T