Canonical Allele Identifier: CA380684502

Gene: TMEM216

Linked Data

• MyVariant Identifiers: chr11:g.61160128G>C (hg19) ; chr11:g.61392656G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392656G>C , CM000673.2:g.61392656G>C	GRCh38
NC_000011.9:g.61160128G>C , CM000673.1:g.61160128G>C	GRCh37
NC_000011.8:g.60916704G>C	NCBI36
NG_032976.1:g.5297G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.10:c.25G>C	ENSP00000334844.5:p.Ala9Pro
ENST00000544795.6:n.70G>C
ENST00000684926.1:n.27G>C
ENST00000688959.1:c.-249G>C	ENSP00000509213.1:n.-249G>C
ENST00000690736.1:c.25G>C	ENSP00000508542.1:p.Ala9Pro
ENST00000515837.7:c.25G>C MANE Select	ENSP00000440638.1:p.Ala9Pro
ENST00000334888.9:c.25G>C	ENSP00000334844.5:p.Ala9Pro
ENST00000398979.7:c.-173G>C	ENSP00000381950.3:n.-173G>C
ENST00000515837.6:c.25G>C	ENSP00000440638.1:p.Ala9Pro
ENST00000541473.1:n.25G>C
ENST00000544795.5:n.27G>C
NM_001173990.2:c.25G>C	NP_001167461.1:p.Ala9Pro
NM_001173991.2:c.25G>C	NP_001167462.1:p.Ala9Pro
NM_016499.5:c.-173G>C	NP_057583.2:n.-173G>C
XM_005274039.3:c.-307G>C	XP_005274096.1:n.-307G>C
NM_001330285.1:c.-173G>C	NP_001317214.1:n.-173G>C
XM_005274039.4:c.-307G>C	XP_005274096.1:n.-307G>C
NM_001173990.3:c.25G>C MANE Select	NP_001167461.1:p.Ala9Pro
NM_001173991.3:c.25G>C	NP_001167462.1:p.Ala9Pro
NM_001330285.2:c.-173G>C	NP_001317214.1:n.-173G>C
NM_016499.6:c.-173G>C	NP_057583.2:n.-173G>C