Canonical Allele Identifier: CA2613835895

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392377-GGTAGTCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392379_61392385del , CM000673.2:g.61392379_61392385del	GRCh38
NC_000011.9:g.61159851_61159857del , CM000673.1:g.61159851_61159857del	GRCh37
NC_000011.8:g.60916427_60916433del	NCBI36
NG_032976.1:g.5020_5026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334888.9:c.-253_-247del	ENSP00000334844.5:n.-253_-247del
ENST00000515837.6:c.-253_-247del	ENSP00000440638.1:n.-253_-247del
NM_001173990.2:c.-253_-247del	NP_001167461.1:n.-253_-247del
NM_001173991.2:c.-253_-247del	NP_001167462.1:n.-253_-247del
XM_005274039.3:c.-584_-578del	XP_005274096.1:n.-584_-578del
NM_001330285.1:c.-450_-444del	NP_001317214.1:n.-450_-444del
XM_005274039.4:c.-584_-578del	XP_005274096.1:n.-584_-578del