Canonical Allele Identifier: CA1272522632

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96255119G= , CM000664.2:g.96255119G=	GRCh38
NC_000002.11:g.96920857G= , CM000664.1:g.96920857G=	GRCh37
NC_000002.10:g.96284584G=	NCBI36
NG_027695.1:g.15895C= , LRG_528:g.15895C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.245-122C= MANE Select	ENSP00000258439.3:n.245-122C=
ENST00000258439.7:c.245-122C=	ENSP00000258439.2:n.245-122C=
ENST00000432959.1:c.245-122C=	ENSP00000416660.1:n.245-122C=
ENST00000435268.1:c.-8-122C=	ENSP00000411810.1:n.-8-122C=
NM_001193304.2:c.245-122C=	NP_001180233.1:n.245-122C=
NM_017849.3:c.245-122C= , LRG_528t1:c.245-122C=	NP_060319.1:n.245-122C=
XM_017004450.1:c.-674-122C=	XP_016859939.1:n.-674-122C=
XM_017004452.1:c.-8-122C=	XP_016859941.1:n.-8-122C=
NM_001193304.3:c.245-122C=	NP_001180233.1:n.245-122C=
NM_017849.4:c.245-122C= MANE Select	NP_060319.1:n.245-122C=