Canonical Allele Identifier: CA474518918
Gene: TMEM216 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.61161369A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61393897A>C , CM000673.2:g.61393897A>C GRCh38
NC_000011.9:g.61161369A>C , CM000673.1:g.61161369A>C GRCh37
NC_000011.8:g.60917945A>C NCBI36
NG_032976.1:g.6538A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000334888.10:c.150A>C ENSP00000334844.5:p.Pro50=
ENST00000544795.6:n.427A>C
ENST00000684926.1:n.166A>C
ENST00000688959.1:c.-110A>C ENSP00000509213.1:n.-110A>C
ENST00000690736.1:c.150A>C ENSP00000508542.1:p.Pro50=
ENST00000515837.7:c.150A>C MANE Select ENSP00000440638.1:p.Pro50=
ENST00000334888.9:c.150A>C ENSP00000334844.5:p.Pro50=
ENST00000398979.7:c.-34A>C ENSP00000381950.3:n.-34A>C
ENST00000515837.6:c.150A>C ENSP00000440638.1:p.Pro50=
ENST00000541473.1:n.164A>C
ENST00000544795.5:n.166A>C
NM_001173990.2:c.150A>C NP_001167461.1:p.Pro50=
NM_001173991.2:c.150A>C NP_001167462.1:p.Pro50=
NM_016499.5:c.-34A>C NP_057583.2:n.-34A>C
XM_005274039.3:c.-34A>C XP_005274096.1:n.-34A>C
NM_001330285.1:c.-34A>C NP_001317214.1:n.-34A>C
XM_005274039.4:c.-34A>C XP_005274096.1:n.-34A>C
NM_001173990.3:c.150A>C MANE Select NP_001167461.1:p.Pro50=
NM_001173991.3:c.150A>C NP_001167462.1:p.Pro50=
NM_001330285.2:c.-34A>C NP_001317214.1:n.-34A>C
NM_016499.6:c.-34A>C NP_057583.2:n.-34A>C