Canonical Allele Identifier: CA1272521232

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251861_96251864delinsCAGG , CM000664.2:g.96251861_96251864delinsCAGG	GRCh38
NC_000002.11:g.96917599_96917602delinsCAGG , CM000664.1:g.96917599_96917602delinsCAGG	GRCh37
NC_000002.10:g.96281326_96281329delinsCAGG	NCBI36
NG_027695.1:g.19150_19153delinsCCTG , LRG_528:g.19150_19153delinsCCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*1944_*1947delinsCCTG MANE Select	ENSP00000258439.3:n.*1944_*1947delinsCCTG
ENST00000258439.7:c.*1944_*1947delinsCCTG	ENSP00000258439.2:n.*1944_*1947delinsCCTG
ENST00000432959.1:c.*1944_*1947delinsCCTG	ENSP00000416660.1:n.*1944_*1947delinsCCTG
NM_001193304.2:c.*1944_*1947delinsCCTG	NP_001180233.1:n.*1944_*1947delinsCCTG
NM_017849.3:c.*1944_*1947delinsCCTG , LRG_528t1:c.*1944_*1947delinsCCTG	NP_060319.1:n.*1944_*1947delinsCCTG
XM_017004450.1:c.*1245_*1248delinsCCTG	XP_016859939.1:n.*1245_*1248delinsCCTG
XM_017004452.1:c.*1944_*1947delinsCCTG	XP_016859941.1:n.*1944_*1947delinsCCTG
NM_001193304.3:c.*1944_*1947delinsCCTG	NP_001180233.1:n.*1944_*1947delinsCCTG
NM_017849.4:c.*1944_*1947delinsCCTG MANE Select	NP_060319.1:n.*1944_*1947delinsCCTG