Canonical Allele Identifier: CA2724156632

Gene: TMEM216

Linked Data

• dbSNP Id: rs2135189093

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392629C>A , CM000673.2:g.61392629C>A	GRCh38
NC_000011.9:g.61160101C>A , CM000673.1:g.61160101C>A	GRCh37
NC_000011.8:g.60916677C>A	NCBI36
NG_032976.1:g.5270C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.-3C>A	ENSP00000334844.5:n.-3C>A
ENST00000544795.6:n.43C>A
ENST00000688959.1:c.-276C>A	ENSP00000509213.1:n.-276C>A
ENST00000690736.1:c.-3C>A	ENSP00000508542.1:n.-3C>A
ENST00000515837.7:c.-3C>A MANE Select	ENSP00000440638.1:n.-3C>A
ENST00000334888.9:c.-3C>A	ENSP00000334844.5:n.-3C>A
ENST00000398979.7:c.-200C>A	ENSP00000381950.3:n.-200C>A
ENST00000515837.6:c.-3C>A	ENSP00000440638.1:n.-3C>A
NM_001173990.2:c.-3C>A	NP_001167461.1:n.-3C>A
NM_001173991.2:c.-3C>A	NP_001167462.1:n.-3C>A
NM_016499.5:c.-200C>A	NP_057583.2:n.-200C>A
XM_005274039.3:c.-334C>A	XP_005274096.1:n.-334C>A
NM_001330285.1:c.-200C>A	NP_001317214.1:n.-200C>A
XM_005274039.4:c.-334C>A	XP_005274096.1:n.-334C>A
NM_001173990.3:c.-3C>A MANE Select	NP_001167461.1:n.-3C>A
NM_001173991.3:c.-3C>A	NP_001167462.1:n.-3C>A
NM_001330285.2:c.-200C>A	NP_001317214.1:n.-200C>A
NM_016499.6:c.-200C>A	NP_057583.2:n.-200C>A