Canonical Allele Identifier: CA6034687

Gene: TMEM216

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392608C>T , CM000673.2:g.61392608C>T	GRCh38
NC_000011.9:g.61160080C>T , CM000673.1:g.61160080C>T	GRCh37
NC_000011.8:g.60916656C>T	NCBI36
NG_032976.1:g.5249C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-24C>T	ENSP00000334844.5:n.-24C>T
ENST00000544795.6:n.22C>T
ENST00000690736.1:c.-24C>T	ENSP00000508542.1:n.-24C>T
ENST00000515837.7:c.-24C>T MANE Select	ENSP00000440638.1:n.-24C>T
ENST00000334888.9:c.-24C>T	ENSP00000334844.5:n.-24C>T
ENST00000398979.7:c.-221C>T	ENSP00000381950.3:n.-221C>T
ENST00000515837.6:c.-24C>T	ENSP00000440638.1:n.-24C>T
NM_001173990.2:c.-24C>T	NP_001167461.1:n.-24C>T
NM_001173991.2:c.-24C>T	NP_001167462.1:n.-24C>T
NM_016499.5:c.-221C>T	NP_057583.2:n.-221C>T
XM_005274039.3:c.-355C>T	XP_005274096.1:n.-355C>T
NM_001330285.1:c.-221C>T	NP_001317214.1:n.-221C>T
XM_005274039.4:c.-355C>T	XP_005274096.1:n.-355C>T
NM_001173990.3:c.-24C>T MANE Select	NP_001167461.1:n.-24C>T
NM_001173991.3:c.-24C>T	NP_001167462.1:n.-24C>T
NM_001330285.2:c.-221C>T	NP_001317214.1:n.-221C>T
NM_016499.6:c.-221C>T	NP_057583.2:n.-221C>T