Canonical Allele Identifier: CA1272521073

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251537_96251538delinsGA , CM000664.2:g.96251537_96251538delinsGA	GRCh38
NC_000002.11:g.96917275_96917276delinsGA , CM000664.1:g.96917275_96917276delinsGA	GRCh37
NC_000002.10:g.96281002_96281003delinsGA	NCBI36
NG_027695.1:g.19476_19477delinsTC , LRG_528:g.19476_19477delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000258439.8:c.*2270_*2271delinsTC MANE Select	ENSP00000258439.3:n.*2270_*2271delinsTC
ENST00000258439.7:c.*2270_*2271delinsTC	ENSP00000258439.2:n.*2270_*2271delinsTC
NM_001193304.2:c.*2270_*2271delinsTC	NP_001180233.1:n.*2270_*2271delinsTC
NM_017849.3:c.*2270_*2271delinsTC , LRG_528t1:c.*2270_*2271delinsTC	NP_060319.1:n.*2270_*2271delinsTC
XM_017004450.1:c.*1571_*1572delinsTC	XP_016859939.1:n.*1571_*1572delinsTC
XM_017004452.1:c.*2270_*2271delinsTC	XP_016859941.1:n.*2270_*2271delinsTC
NM_001193304.3:c.*2270_*2271delinsTC	NP_001180233.1:n.*2270_*2271delinsTC
NM_017849.4:c.*2270_*2271delinsTC MANE Select	NP_060319.1:n.*2270_*2271delinsTC