Canonical Allele Identifier: CA1272521189

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96251780G= , CM000664.2:g.96251780G=	GRCh38
NC_000002.11:g.96917518G= , CM000664.1:g.96917518G=	GRCh37
NC_000002.10:g.96281245G=	NCBI36
NG_027695.1:g.19234C= , LRG_528:g.19234C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.*2028C= MANE Select	ENSP00000258439.3:n.*2028C=
ENST00000258439.7:c.*2028C=	ENSP00000258439.2:n.*2028C=
ENST00000432959.1:c.*2028C=	ENSP00000416660.1:n.*2028C=
NM_001193304.2:c.*2028C=	NP_001180233.1:n.*2028C=
NM_017849.3:c.*2028C= , LRG_528t1:c.*2028C=	NP_060319.1:n.*2028C=
XM_017004450.1:c.*1329C=	XP_016859939.1:n.*1329C=
XM_017004452.1:c.*2028C=	XP_016859941.1:n.*2028C=
NM_001193304.3:c.*2028C=	NP_001180233.1:n.*2028C=
NM_017849.4:c.*2028C= MANE Select	NP_060319.1:n.*2028C=