Canonical Allele Identifier: CA2613839139

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61397715-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61397715T>C , CM000673.2:g.61397715T>C	GRCh38
NC_000011.9:g.61165187T>C , CM000673.1:g.61165187T>C	GRCh37
NC_000011.8:g.60921763T>C	NCBI36
NG_032976.1:g.10356T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000334888.10:c.230-59T>C	ENSP00000334844.5:n.230-59T>C
ENST00000544795.6:n.507-13T>C
ENST00000684926.1:n.246-13T>C
ENST00000688959.1:c.-21-67T>C	ENSP00000509213.1:n.-21-67T>C
ENST00000690736.1:c.230-13T>C	ENSP00000508542.1:n.230-13T>C
ENST00000515837.7:c.230-59T>C MANE Select	ENSP00000440638.1:n.230-59T>C
ENST00000334888.9:c.230-59T>C	ENSP00000334844.5:n.230-59T>C
ENST00000398979.7:c.47-59T>C	ENSP00000381950.3:n.47-59T>C
ENST00000515837.6:c.230-59T>C	ENSP00000440638.1:n.230-59T>C
ENST00000544795.5:n.246-13T>C
NM_001173990.2:c.230-59T>C	NP_001167461.1:n.230-59T>C
NM_001173991.2:c.230-59T>C	NP_001167462.1:n.230-59T>C
NM_016499.5:c.47-59T>C	NP_057583.2:n.47-59T>C
XM_005274039.3:c.47-59T>C	XP_005274096.1:n.47-59T>C
NM_001330285.1:c.47-59T>C	NP_001317214.1:n.47-59T>C
XM_005274039.4:c.47-59T>C	XP_005274096.1:n.47-59T>C
NM_001173990.3:c.230-59T>C MANE Select	NP_001167461.1:n.230-59T>C
NM_001173991.3:c.230-59T>C	NP_001167462.1:n.230-59T>C
NM_001330285.2:c.47-59T>C	NP_001317214.1:n.47-59T>C
NM_016499.6:c.47-59T>C	NP_057583.2:n.47-59T>C