Canonical Allele Identifier: CA1272522589

Gene: TMEM127

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96255023C= , CM000664.2:g.96255023C=	GRCh38
NC_000002.11:g.96920761C= , CM000664.1:g.96920761C=	GRCh37
NC_000002.10:g.96284488C=	NCBI36
NG_027695.1:g.15991G= , LRG_528:g.15991G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258439.8:c.245-26G= MANE Select	ENSP00000258439.3:n.245-26G=
ENST00000258439.7:c.245-26G=	ENSP00000258439.2:n.245-26G=
ENST00000432959.1:c.245-26G=	ENSP00000416660.1:n.245-26G=
ENST00000435268.1:c.-8-26G=	ENSP00000411810.1:n.-8-26G=
NM_001193304.2:c.245-26G=	NP_001180233.1:n.245-26G=
NM_017849.3:c.245-26G= , LRG_528t1:c.245-26G=	NP_060319.1:n.245-26G=
XM_017004450.1:c.-674-26G=	XP_016859939.1:n.-674-26G=
XM_017004452.1:c.-8-26G=	XP_016859941.1:n.-8-26G=
NM_001193304.3:c.245-26G=	NP_001180233.1:n.245-26G=
NM_017849.4:c.245-26G= MANE Select	NP_060319.1:n.245-26G=