Canonical Allele Identifier: CA1272520855

Gene: TMEM127

Linked Data

• dbSNP Id: rs1684077469
• gnomAD v4: 2-96251065-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251068del , CM000664.2:g.96251068del	GRCh38
NC_000002.11:g.96916806del , CM000664.1:g.96916806del	GRCh37
NC_000002.10:g.96280533del	NCBI36
NG_027695.1:g.19948del , LRG_528:g.19948del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2742del MANE Select	ENSP00000258439.3:n.*2742del
ENST00000258439.7:c.*2742del	ENSP00000258439.2:n.*2742del
NM_001193304.2:c.*2742del	NP_001180233.1:n.*2742del
NM_017849.3:c.*2742del , LRG_528t1:c.*2742del	NP_060319.1:n.*2742del
XM_017004450.1:c.*2043del	XP_016859939.1:n.*2043del
XM_017004452.1:c.*2742del	XP_016859941.1:n.*2742del
NM_001193304.3:c.*2742del	NP_001180233.1:n.*2742del
NM_017849.4:c.*2742del MANE Select	NP_060319.1:n.*2742del