Canonical Allele Identifier: CA1272521463
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96252406G= , CM000664.2:g.96252406G= GRCh38
NC_000002.11:g.96918144G= , CM000664.1:g.96918144G= GRCh37
NC_000002.10:g.96281871G= NCBI36
NG_027695.1:g.18608C= , LRG_528:g.18608C=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*1402C= MANE Select ENSP00000258439.3:n.*1402C=
ENST00000258439.7:c.*1402C= ENSP00000258439.2:n.*1402C=
ENST00000432959.1:c.*1402C= ENSP00000416660.1:n.*1402C=
NM_001193304.2:c.*1402C= NP_001180233.1:n.*1402C=
NM_017849.3:c.*1402C= , LRG_528t1:c.*1402C= NP_060319.1:n.*1402C=
XM_017004450.1:c.*703C= XP_016859939.1:n.*703C=
XM_017004452.1:c.*1402C= XP_016859941.1:n.*1402C=
NM_001193304.3:c.*1402C= NP_001180233.1:n.*1402C=
NM_017849.4:c.*1402C= MANE Select NP_060319.1:n.*1402C=