Canonical Allele Identifier: CA1272522123

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96254029C= , CM000664.2:g.96254029C=	GRCh38
NC_000002.11:g.96919767C= , CM000664.1:g.96919767C=	GRCh37
NC_000002.10:g.96283494C=	NCBI36
NG_027695.1:g.16985G= , LRG_528:g.16985G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.496G= MANE Select	ENSP00000258439.3:p.Gly166=
ENST00000258439.7:c.496G=	ENSP00000258439.2:p.Gly166=
ENST00000432959.1:c.496G=	ENSP00000416660.1:p.Gly166=
ENST00000435268.1:c.244G=	ENSP00000411810.1:p.Gly82=
NM_001193304.2:c.496G=	NP_001180233.1:p.Gly166=
NM_017849.3:c.496G= , LRG_528t1:c.496G=	NP_060319.1:p.Gly166=
XM_017004450.1:c.-423G=	XP_016859939.1:n.-423G=
XM_017004452.1:c.244G=	XP_016859941.1:p.Gly82=
NM_001193304.3:c.496G=	NP_001180233.1:p.Gly166=
NM_017849.4:c.496G= MANE Select	NP_060319.1:p.Gly166=