Canonical Allele Identifier: CA2613835992

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392425-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392425C>A , CM000673.2:g.61392425C>A	GRCh38
NC_000011.9:g.61159897C>A , CM000673.1:g.61159897C>A	GRCh37
NC_000011.8:g.60916473C>A	NCBI36
NG_032976.1:g.5066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-207C>A	ENSP00000334844.5:n.-207C>A
ENST00000398979.7:c.-404C>A	ENSP00000381950.3:n.-404C>A
ENST00000515837.6:c.-207C>A	ENSP00000440638.1:n.-207C>A
NM_001173990.2:c.-207C>A	NP_001167461.1:n.-207C>A
NM_001173991.2:c.-207C>A	NP_001167462.1:n.-207C>A
NM_016499.5:c.-404C>A	NP_057583.2:n.-404C>A
XM_005274039.3:c.-538C>A	XP_005274096.1:n.-538C>A
NM_001330285.1:c.-404C>A	NP_001317214.1:n.-404C>A
XM_005274039.4:c.-538C>A	XP_005274096.1:n.-538C>A