Canonical Allele Identifier: CA2574840928

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392612G>T , CM000673.2:g.61392612G>T	GRCh38
NC_000011.9:g.61160084G>T , CM000673.1:g.61160084G>T	GRCh37
NC_000011.8:g.60916660G>T	NCBI36
NG_032976.1:g.5253G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-20G>T	ENSP00000334844.5:n.-20G>T
ENST00000544795.6:n.26G>T
ENST00000690736.1:c.-20G>T	ENSP00000508542.1:n.-20G>T
ENST00000515837.7:c.-20G>T MANE Select	ENSP00000440638.1:n.-20G>T
ENST00000334888.9:c.-20G>T	ENSP00000334844.5:n.-20G>T
ENST00000398979.7:c.-217G>T	ENSP00000381950.3:n.-217G>T
ENST00000515837.6:c.-20G>T	ENSP00000440638.1:n.-20G>T
NM_001173990.2:c.-20G>T	NP_001167461.1:n.-20G>T
NM_001173991.2:c.-20G>T	NP_001167462.1:n.-20G>T
NM_016499.5:c.-217G>T	NP_057583.2:n.-217G>T
XM_005274039.3:c.-351G>T	XP_005274096.1:n.-351G>T
NM_001330285.1:c.-217G>T	NP_001317214.1:n.-217G>T
XM_005274039.4:c.-351G>T	XP_005274096.1:n.-351G>T
NM_001173990.3:c.-20G>T MANE Select	NP_001167461.1:n.-20G>T
NM_001173991.3:c.-20G>T	NP_001167462.1:n.-20G>T
NM_001330285.2:c.-217G>T	NP_001317214.1:n.-217G>T
NM_016499.6:c.-217G>T	NP_057583.2:n.-217G>T