Canonical Allele Identifier: CA2792320036

Gene: TMEM216

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392520_61392521insCGGCCTC , CM000673.2:g.61392520_61392521insCGGCCTC	GRCh38
NC_000011.9:g.61159992_61159993insCGGCCTC , CM000673.1:g.61159992_61159993insCGGCCTC	GRCh37
NC_000011.8:g.60916568_60916569insCGGCCTC	NCBI36
NG_032976.1:g.5161_5162insCGGCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-112_-111insCGGCCTC	ENSP00000334844.5:n.-112_-111insCGGCCTC
ENST00000398979.7:c.-309_-308insCGGCCTC	ENSP00000381950.3:n.-309_-308insCGGCCTC
ENST00000515837.6:c.-112_-111insCGGCCTC	ENSP00000440638.1:n.-112_-111insCGGCCTC
NM_001173990.2:c.-112_-111insCGGCCTC	NP_001167461.1:n.-112_-111insCGGCCTC
NM_001173991.2:c.-112_-111insCGGCCTC	NP_001167462.1:n.-112_-111insCGGCCTC
NM_016499.5:c.-309_-308insCGGCCTC	NP_057583.2:n.-309_-308insCGGCCTC
XM_005274039.3:c.-443_-442insCGGCCTC	XP_005274096.1:n.-443_-442insCGGCCTC
NM_001330285.1:c.-309_-308insCGGCCTC	NP_001317214.1:n.-309_-308insCGGCCTC
XM_005274039.4:c.-443_-442insCGGCCTC	XP_005274096.1:n.-443_-442insCGGCCTC