Canonical Allele Identifier: CA2660175447

Gene: TMEM127

Linked Data

• gnomAD v4: 2-96251742-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251742T>A , CM000664.2:g.96251742T>A	GRCh38
NC_000002.11:g.96917480T>A , CM000664.1:g.96917480T>A	GRCh37
NC_000002.10:g.96281207T>A	NCBI36
NG_027695.1:g.19272A>T , LRG_528:g.19272A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2066A>T MANE Select	ENSP00000258439.3:n.*2066A>T
ENST00000258439.7:c.*2066A>T	ENSP00000258439.2:n.*2066A>T
ENST00000432959.1:c.*2066A>T	ENSP00000416660.1:n.*2066A>T
NM_001193304.2:c.*2066A>T	NP_001180233.1:n.*2066A>T
NM_017849.3:c.*2066A>T , LRG_528t1:c.*2066A>T	NP_060319.1:n.*2066A>T
XM_017004450.1:c.*1367A>T	XP_016859939.1:n.*1367A>T
XM_017004452.1:c.*2066A>T	XP_016859941.1:n.*2066A>T
NM_001193304.3:c.*2066A>T	NP_001180233.1:n.*2066A>T
NM_017849.4:c.*2066A>T MANE Select	NP_060319.1:n.*2066A>T