Canonical Allele Identifier: CA2660178485

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96255120-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96255122_96255123del , CM000664.2:g.96255122_96255123del	GRCh38
NC_000002.11:g.96920860_96920861del , CM000664.1:g.96920860_96920861del	GRCh37
NC_000002.10:g.96284587_96284588del	NCBI36
NG_027695.1:g.15892_15893del , LRG_528:g.15892_15893del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.245-125_245-124del MANE Select	ENSP00000258439.3:n.245-125_245-124del
ENST00000258439.7:c.245-125_245-124del	ENSP00000258439.2:n.245-125_245-124del
ENST00000432959.1:c.245-125_245-124del	ENSP00000416660.1:n.245-125_245-124del
ENST00000435268.1:c.-8-125_-8-124del	ENSP00000411810.1:n.-8-125_-8-124del
NM_001193304.2:c.245-125_245-124del	NP_001180233.1:n.245-125_245-124del
NM_017849.3:c.245-125_245-124del , LRG_528t1:c.245-125_245-124del	NP_060319.1:n.245-125_245-124del
XM_017004450.1:c.-674-125_-674-124del	XP_016859939.1:n.-674-125_-674-124del
XM_017004452.1:c.-8-125_-8-124del	XP_016859941.1:n.-8-125_-8-124del
NM_001193304.3:c.245-125_245-124del	NP_001180233.1:n.245-125_245-124del
NM_017849.4:c.245-125_245-124del MANE Select	NP_060319.1:n.245-125_245-124del