Canonical Allele Identifier: CA1272521461
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96252402C= , CM000664.2:g.96252402C= GRCh38
NC_000002.11:g.96918140C= , CM000664.1:g.96918140C= GRCh37
NC_000002.10:g.96281867C= NCBI36
NG_027695.1:g.18612G= , LRG_528:g.18612G=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*1406G= MANE Select ENSP00000258439.3:n.*1406G=
ENST00000258439.7:c.*1406G= ENSP00000258439.2:n.*1406G=
ENST00000432959.1:c.*1406G= ENSP00000416660.1:n.*1406G=
NM_001193304.2:c.*1406G= NP_001180233.1:n.*1406G=
NM_017849.3:c.*1406G= , LRG_528t1:c.*1406G= NP_060319.1:n.*1406G=
XM_017004450.1:c.*707G= XP_016859939.1:n.*707G=
XM_017004452.1:c.*1406G= XP_016859941.1:n.*1406G=
NM_001193304.3:c.*1406G= NP_001180233.1:n.*1406G=
NM_017849.4:c.*1406G= MANE Select NP_060319.1:n.*1406G=