Canonical Allele Identifier: CA2792320026
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61392489G>T , CM000673.2:g.61392489G>T GRCh38
NC_000011.9:g.61159961G>T , CM000673.1:g.61159961G>T GRCh37
NC_000011.8:g.60916537G>T NCBI36
NG_032976.1:g.5130G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.9:c.-143G>T ENSP00000334844.5:n.-143G>T
ENST00000398979.7:c.-340G>T ENSP00000381950.3:n.-340G>T
ENST00000515837.6:c.-143G>T ENSP00000440638.1:n.-143G>T
NM_001173990.2:c.-143G>T NP_001167461.1:n.-143G>T
NM_001173991.2:c.-143G>T NP_001167462.1:n.-143G>T
NM_016499.5:c.-340G>T NP_057583.2:n.-340G>T
XM_005274039.3:c.-474G>T XP_005274096.1:n.-474G>T
NM_001330285.1:c.-340G>T NP_001317214.1:n.-340G>T
XM_005274039.4:c.-474G>T XP_005274096.1:n.-474G>T