Canonical Allele Identifier: CA2660178329

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96254999-T-TTTCAGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254999_96255000insTTCAGCAG , CM000664.2:g.96254999_96255000insTTCAGCAG	GRCh38
NC_000002.11:g.96920737_96920738insTTCAGCAG , CM000664.1:g.96920737_96920738insTTCAGCAG	GRCh37
NC_000002.10:g.96284464_96284465insTTCAGCAG	NCBI36
NG_027695.1:g.16014_16015insCTGCTGAA , LRG_528:g.16014_16015insCTGCTGAA

Transcript Alleles

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