Canonical Allele Identifier: CA1272520640
Gene: TMEM127 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.96250623T= , CM000664.2:g.96250623T= GRCh38
NC_000002.11:g.96916361T= , CM000664.1:g.96916361T= GRCh37
NC_000002.10:g.96280088T= NCBI36
NG_027695.1:g.20391A= , LRG_528:g.20391A=

Transcript Alleles

HGVS Amino-acid change
ENST00000258439.8:c.*3185A= MANE Select ENSP00000258439.3:n.*3185A=
ENST00000258439.7:c.*3185A= ENSP00000258439.2:n.*3185A=
NM_001193304.2:c.*3185A= NP_001180233.1:n.*3185A=
NM_017849.3:c.*3185A= , LRG_528t1:c.*3185A= NP_060319.1:n.*3185A=
XM_017004450.1:c.*2486A= XP_016859939.1:n.*2486A=
XM_017004452.1:c.*3185A= XP_016859941.1:n.*3185A=
NM_001193304.3:c.*3185A= NP_001180233.1:n.*3185A=
NM_017849.4:c.*3185A= MANE Select NP_060319.1:n.*3185A=