Canonical Allele Identifier: CA2613835800

Gene: TMEM216

Linked Data

• gnomAD v4: 11-61392276-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61392280del , CM000673.2:g.61392280del	GRCh38
NC_000011.9:g.61159752del , CM000673.1:g.61159752del	GRCh37
NC_000011.8:g.60916328del	NCBI36
NG_032976.1:g.4921del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000515837.6:c.-352del	ENSP00000440638.1:n.-352del
XM_005274039.3:c.-683del	XP_005274096.1:n.-683del
XM_005274039.4:c.-683del	XP_005274096.1:n.-683del