Canonical Allele Identifier: CA2660174860

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96250689-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96250689C>A , CM000664.2:g.96250689C>A	GRCh38
NC_000002.11:g.96916427C>A , CM000664.1:g.96916427C>A	GRCh37
NC_000002.10:g.96280154C>A	NCBI36
NG_027695.1:g.20325G>T , LRG_528:g.20325G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*3119G>T MANE Select	ENSP00000258439.3:n.*3119G>T
ENST00000258439.7:c.*3119G>T	ENSP00000258439.2:n.*3119G>T
NM_001193304.2:c.*3119G>T	NP_001180233.1:n.*3119G>T
NM_017849.3:c.*3119G>T , LRG_528t1:c.*3119G>T	NP_060319.1:n.*3119G>T
XM_017004450.1:c.*2420G>T	XP_016859939.1:n.*2420G>T
XM_017004452.1:c.*3119G>T	XP_016859941.1:n.*3119G>T
NM_001193304.3:c.*3119G>T	NP_001180233.1:n.*3119G>T
NM_017849.4:c.*3119G>T MANE Select	NP_060319.1:n.*3119G>T