Canonical Allele Identifier: CA1272526985

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96265229G= , CM000664.2:g.96265229G=	GRCh38
NC_000002.11:g.96930967G= , CM000664.1:g.96930967G=	GRCh37
NC_000002.10:g.96294694G=	NCBI36
NG_027695.1:g.5785C= , LRG_528:g.5785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.153C= MANE Select	ENSP00000258439.3:p.Pro51=
ENST00000258439.7:c.153C=	ENSP00000258439.2:p.Pro51=
ENST00000432959.1:c.153C=	ENSP00000416660.1:p.Pro51=
NM_001193304.2:c.153C=	NP_001180233.1:p.Pro51=
NM_017849.3:c.153C= , LRG_528t1:c.153C=	NP_060319.1:p.Pro51=
NM_001193304.3:c.153C=	NP_001180233.1:p.Pro51=
NM_017849.4:c.153C= MANE Select	NP_060319.1:p.Pro51=