Canonical Allele Identifier: CA1977296212
Gene: TMEM216 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61393048G= , CM000673.2:g.61393048G= GRCh38
NC_000011.9:g.61160520G= , CM000673.1:g.61160520G= GRCh37
NC_000011.8:g.60917096G= NCBI36
NG_032976.1:g.5689G=

Transcript Alleles

HGVS Amino-acid change
ENST00000334888.10:c.35-183G= ENSP00000334844.5:n.35-183G=
ENST00000544795.6:n.311+151G=
ENST00000684926.1:n.51-183G=
ENST00000688959.1:c.-225-183G= ENSP00000509213.1:n.-225-183G=
ENST00000690736.1:c.35-183G= ENSP00000508542.1:n.35-183G=
ENST00000515837.7:c.35-183G= MANE Select ENSP00000440638.1:n.35-183G=
ENST00000334888.9:c.35-183G= ENSP00000334844.5:n.35-183G=
ENST00000398979.7:c.-149-183G= ENSP00000381950.3:n.-149-183G=
ENST00000515837.6:c.35-183G= ENSP00000440638.1:n.35-183G=
ENST00000541473.1:n.49-183G=
ENST00000544795.5:n.51-183G=
NM_001173990.2:c.35-183G= NP_001167461.1:n.35-183G=
NM_001173991.2:c.35-183G= NP_001167462.1:n.35-183G=
NM_016499.5:c.-149-183G= NP_057583.2:n.-149-183G=
XM_005274039.3:c.-150+151G= XP_005274096.1:n.-150+151G=
NM_001330285.1:c.-149-183G= NP_001317214.1:n.-149-183G=
XM_005274039.4:c.-150+151G= XP_005274096.1:n.-150+151G=
NM_001173990.3:c.35-183G= MANE Select NP_001167461.1:n.35-183G=
NM_001173991.3:c.35-183G= NP_001167462.1:n.35-183G=
NM_001330285.2:c.-149-183G= NP_001317214.1:n.-149-183G=
NM_016499.6:c.-149-183G= NP_057583.2:n.-149-183G=